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Every new U.S. recall of food, medicines, medical devices and household products, in one place, updated every day. Search for a product or brand you own.

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Latest recalls

Consumer products · Sep 17, 2026

Melissa & Doug Recalls Fire Truck Activity Board Toys Due to Risk of Serious Injury from Choking Hazard; Sold Exclusively at Target

Melissa & Doug, of Wilton, Connecticut · China

Why: The fire hose port can come loose and detach, posing a risk of serious injury from choking hazard.

Product details, where it was sold and what to do

Lights & Sounds Fire Truck Activity Board. The "Lights and Sound Fire Truck" is a compact fire engine toy with wheels that spin, that also features busy board activities that activate lights and sounds. The toy is made of red plastic, has four black wheels and has a white plastic rotating ladder. The toy has a black plastic connector that looks like a fire hose. The toy measures 10.5 inches high by 14.31 inches wide by 3.06 inches deep and weighs about 1.6 pounds. On the bottom of the toy, "Melissa & Doug" is embossed on the battery compartment box as are two date wheels showing the dates of manufacturer by year and month. Affected units will have one arrow pointing to the number 25 and the second arrow pointing to the number 4 or 5 or they will have one arrow pointing to the number 26 and the second arrow pointing to the number 3. Date codes OET 25100, OET 25150 or OET 26064 are printed on the product packaging of the recalled units.

Quantity: About 84,000

Distribution: Sold at Sold At: Target stores nationwide and online at Target.com from July 2025 through August 2026 for about $30.

Remedy: Consumers should stop using the fire truck activity board immediately and register at www.melissaanddoug.com/recall for instructions on how to receive a free replacement fire truck activity board, register for a full refund of $30 in the form of a check or receive a $40 melissaanddoug.com store credit. Consumers will be asked to remove the batteries, write in permanent marker the word “RECALL” on

Official CPSC recall notice ↗

Consumer products · Sep 17, 2026

LANCHEZ Pressure Washers Recalled Due to Serious Risk of Injury or Death from Shock and Electrocution Hazards

Ningbo Lanchez E-Commerce Co., Ltd. of China · China

Why: The recalled pressure washers lack an integral ground-fault circuit-interrupter (GFCI) and an adequate-length power cord, which may encourage use of an extension cord, posing serious risks of injury or death from shock and electrocution hazards.

Product details, where it was sold and what to do

LANCHEZ Pressure Washers. This recall involves LANCHEZ-branded pressure washers. The recalled, 3.2 GPM electric pressure washers were sold in blue-and-black or red-and-black, and measure about 12.2 inches deep, 16.9 inches wide and 16.5 inches high. The pressure washers came with a 500 ml soap tank, four quick disconnect nozzles and a 23-foot hose. Only power washers without a GFCI or adequate-length power cord are included in this recall. “LANCHEZ” is printed on the front of the power washer and model number “KLC-BULL135C” is printed on a label on top of the unit near the handle.

Quantity: 329

Distribution: Sold at Sold Online At: Amazon.com, Walmart.com and Temu.com from February 2026 through June 2026 for between $88 and $266.

Remedy: Consumers should stop using the recalled pressure washers immediately and contact LANCHEZ for a full refund. Consumers will be asked to unplug the pressure washer, destroy it by cutting the power cord in half and send a photo of the destroyed power washer, showing the model number, to service@lanchezpumps.com. Consumers should then dispose of the destroyed recalled product.

Official CPSC recall notice ↗

Consumer products · Sep 17, 2026

JKMAX Recalls Heated Blankets and Heating Pads Due to Fire and Burn Hazards

Jiande Pengshuai Trading Co., Ltd, of China · China

Why: The internal wire heating elements of the blankets and pads can overheat, posing fire and burn hazards to consumers.

Product details, where it was sold and what to do

JKMAX Heated Blankets and Heating Pads. This recall involves all heating pads and heated blankets sold by JKMax, including models JKMAX-002, JKMAX-7284B, JKMAX-6284B, JKMAX-10090B, JKMAX-8490B and JKMAX-6284B. The heated blankets and heating pads are blue, gray, brown or red. They are made of polyester fabric and are machine washable. The blankets and pads were sold in multiple sizes, and both have a detachable white remote that can be used to adjust the heat. The model number is located on the back of the remote and is also printed on a white label affixed to the product packaging along with the brand name "JKMAX".

Quantity: About 195,000

Distribution: Sold at Sold Online At: Amazon.com from September 2022 through July 2026 as both a one-pack or a two-pack.

Remedy: Consumers should stop using the recalled blankets and pads immediately and contact JKMax for a full refund.

Official CPSC recall notice ↗

Consumer products · Sep 17, 2026

Hayward Industries Recalls Universal Pool Heaters Due to Risk of Serious Injury or Death from Carbon Monoxide Poisoning Hazard.

Hayward Industries, Inc., of Charlotte, North Carolina · United States

Why: During operation, the heaters can produce high levels of carbon monoxide (CO), posing a risk of serious injury or death from carbon monoxide poisoning.

Product details, where it was sold and what to do

400,000 BTU Universal-HC Series Pool Heaters. This recall involves Hayward-branded HDFS400 Universal-HC Series pool heaters. The 400,000 BTU dual-fuel gas heaters are brown with black atop and measure 21 inches long, 28 inches wide and 31 inches high. The pool heaters have a digital display control panel at the top and a molded base with integrated tie-down connections. The heater's name plate is below the vent with the word "Hayward" appearing at the bottom of the name plate and the model number "HDFS400" appears at the top of the name plate.

Quantity: About 4,600

Distribution: Sold at Sold At: Pool equipment distributors, builders and service professionals nationwide from March 2026 through July 2026 for about $5,600.

Remedy: Consumers should stop using the pool heater immediately and contact Hayward Industries to schedule a free in-home inspection and repair by a qualified technician.

Official CPSC recall notice ↗

Consumer products · Sep 17, 2026

Friedrich Air Conditioning Recalls KÜHL Window Air Conditioners Due to Risk of Serious Injury or Death from Fire and Burn Hazards

Friedrich Air Conditioning Co., of San Antonio, Texas · Mexico

Why: The control board inside the motor of the recalled air conditioners can fail, posing a risk of serious injury or death from fire and burn hazards.

Product details, where it was sold and what to do

Kühl® Q and Kühl® S Window Air Conditioners. This recall involves KÜHL Q and KÜHL S Window Air Conditioners. The products have a gray front and a black air discharge grille and have the name Friedrich and the Friedrich logo in the lower left corner of the unit. The Kühl Q front control panel is located on the top left corner of the unit, and the Kühl S front control panel is located on the right side of the unit below the discharge grille. The models are KCVQ08B10A, KHVQ10B11A, KCVS08B10A, KCVS12B10A, KCVS12B30A and KCVS16B30A. The model and serial number are located inside the air conditioners. Only some serial numbers below have motors that are included in this recall.

Quantity: About 2,000

Distribution: Sold at Sold At: PC Richard & Son, Grainger, and Johnson Supply stores and other appliance distributors and retailers nationwide from January 2026 through August 2026 for between $1,300 and $2,000.

Remedy: Consumers should stop using the recalled air conditioners immediately and visit www.friedrich.com/product-recall to receive information on how to determine if their unit is covered by the recall. Consumers should have the air conditioner’s serial number, which can be found on the inside of the unit, when they visit the recall web page or call Friedrich about the recall. If your unit has a serial n

Official CPSC recall notice ↗

Consumer products · Sep 17, 2026

Esjay US Recalls Toddler Busy Board Montessori Toys Due to Risk of Serious Injury or Death from Choking; Violates Small Parts Ban

Shenzhen Yishijie Technology Co., Ltd., dba Esjay US, of China · China

Why: The recalled toy violates the small parts ban because the product is for children under three years of age and the red knobs can detach, posing a deadly choking hazard.

Product details, where it was sold and what to do

Esjay Toddler Busy Board Montessori Toys. This recall involves Esjay Toddler Busy Board Montessori Toys. The busy boards are made of blue felt, have carrying handles, elastic cords and button closures. The front is printed with various cartoon dinosaurs, and the back is printed with 26 small squares, each corresponding to a letter of the alphabet. Each square contains the letter and a cartoon animal. The busy boards have five pages in total and the page with red knobs is the second page.

Quantity: About 276,000

Distribution: Sold at Sold Online At: Amazon.com from March 2023 to July 2026 for between $18 and $30.

Remedy: Consumers should take the recalled toy away from children, stop using it immediately and contact Esjay for instructions on the repair. Consumers will be asked to unzip the page with red knobs, write “RECALLED” on both sides of the page and throw it away. Send a photo of the disposed page to Esjay US at esjay-service@outlook.com to receive a replacement page.

Official CPSC recall notice ↗

Consumer products · Sep 17, 2026

Colerinsec Recalls Jerify Magnetic Stick Figure Toy Sets Due to Risk of Serious Injury or Death from Magnet Ingestion; Violate Mandatory Standard for Toys

Hefei Hanchan Network Technology Co., Ltd., dba Colerinsec, of China · China

Why: The magnetic humanoid toy Sets violate the mandatory standard for toys because they can liberate loose high-powered magnets posing an ingestion hazard to children. When high-powered magnets are swallowed, the ingested magnets can attract each other or other metal objects and become lodged in the digestive system. This can result in perforations, twisting, and/or blockage of the intestines, blood poisoning and death.

Product details, where it was sold and what to do

Jerify Magnetic Humanoid Toy Sets 30 PCS. This recall involves Jerify Magnetic Humanoid Toys 30 PCS. The 30-piece magnetic toys come in three units of brown, white, green, peach, yellow, pink, blue, orange, purple, and red figures in the shape of a human. Each figure measures about 2.7 inches tall by 2.5 inches wide. The magnetic toys contain magnets in the hand and foot locations. There is no labeling on the product. The magnetic toys come in an unlabeled clear bag enclosed in a brown box with the brand name "Jerify" and number "X003ADA3TD" located on the sticker.

Quantity: About 38,507

Distribution: Sold at Online at Amazon.com from October 2022 through May 2026 for about $21.

Remedy: Consumers should take the magnetic humanoid toys away from children immediately, stop using them and contact Colerinsec for a full refund. Consumers will be asked to throw away the magnetic toys and submit a photo of the disposed toys to coushdwugintwer@163.com.

Official CPSC recall notice ↗

Consumer products · Sep 17, 2026

Char-Broil Recalls Bistro Pro Electric Grills Due to Risk of Electric Shock

Char-Broil LLC, of Columbus, Georgia · China

Why: The grounding wire for the grill's heating element can disconnect and lose fault protection, posing an electric shock hazard.

Product details, where it was sold and what to do

Charbroil Bistro Pro Electric Grills. This recall involves the Charbroil Bistro Pro Electric Grills with model descriptions Bistro Pro Electric Grill & Griddle + Charcoal, Bistro Electric Grill + Charcoal and Bistro Pro Tabletop Electric Grill. The grills were sold in full-size and tabletop configurations in Black (black and gray), Red, Blackout (all black) and Emerald (green). The units have a "CB" logo plate on the front of the lid and "CHARBROIL" printed on the front control panel. The product label listing the model and serial number, including a four-digit manufacturing date code in year and month (YYMM) format, is located on the bottom shelf of full-size grills and on the side bar of tabletop models. Only Bistro Pro Electric Grills with date codes of 2510 (Oct-2025), 2511 (Nov-2025) and 2512 (Dec-2025) are included in this recall. Model Description Model No. Bistro Pro™ Electric Grill & Griddle + Charcoal Mode Black 25302145 Bistro Pro™ Electric Grill & Griddle + Charcoal Mode Red 25302146 Bistro Pro™ Electric Grill + Charcoal Mode Blackout 25302147 Bistro Pro™ Electric Grill + Charcoal Mode Black 25302148 Bistro Pro™ Tabletop Electric Grill Black 25302149 Bistro Pro™ Tabletop Electric Grill Red 25302150 Bistro Pro™ Electric Grill & Griddle + Charcoal Mode Black with Cover 25302151 Bistro Pro™ Electric Grill & Griddle + Charcoal Mode Red with cover 25302159 Bistro Pro™ Electric Grill & Griddle + Charcoal Mode Emerald with cover 25302163

Quantity: About 10,605 (In addition, 342 were sold in Canada)

Distribution: Sold at Ace Hardware, Lowe's, Walmart, Wayfair, QVC and other hardware stores nationwide online at Amazon.com, Charbroil.com, Ace Hardware.com, Lowes.com, Walmart.com, Wayfair.com, QVC.com and other online retailers from October 2025 through June 2026 for between $150 and $250.

Remedy: Consumers should stop using the recalled electric grills immediately and contact Char-Broil for a free repair kit. Consumers will be asked to register at www.charbroil.com/BistroProFix to receive repair instructions, a screwdriver, a wrench, screws and a label to affix to the grill after repair. Char-Broil is offering a digital $25 gift card, valid at participating retailers, to consumers who prov

Official CPSC recall notice ↗

Medical devices · Sep 16, 2026 · Class II · Ongoing

Getinge PVC Thoracic Catheter, Soft PVC Right Angle, 10 per Case

Atrium Medical Corporation · Merrimack, NH, United States

Why: An Out of Specification result (OOS) related to bacterial endotoxin testing in a single lot of catheters.

Product details, where it was sold and what to do

Getinge PVC Thoracic Catheter, Soft PVC Right Angle, 10 per Case; Size(Model Number): 1. 24FR(8124), 2. 28FR(8128), 3. 32FR(8132), 4. 36FR(8136);

Quantity: 2533

Distribution: US Nationwide distribution.

Recall number Z-3112-2026 in the FDA Enforcement Report. Check the lot numbers and dates on your product against the description above.

Medical devices · Sep 16, 2026 · Class II · Ongoing

Products that contain the Pericare Wipes: *Bardex¿ I.C

C.R. Bard Inc · Covington, GA, United States

Why: Due to complaints received indicating presence of contamination on the surface of pericare wipes provided with various Foley and Intermittent Catheter Trays.

Product details, where it was sold and what to do

Products that contain the Pericare Wipes: *Bardex¿ I.C. Complete Care¿ Foley Catheter Tray REF: 300316A UDI codes: 00801741024344¿ 10801741024341 *Bardex¿ I.C. Complete Care¿ Foley Catheter Tray and Urine Meter REF: 303314A 303316A 303318A UDI code: 00801741024252¿ 10801741024259 00801741024269 10801741024266 00801741024276¿ 10801741024273 *SureStep" Foley Tray System Bardex¿ IC Complete Care¿ REF: A300314A UDI codes: 00801741073724¿ 10801741073721 REF: A300314AC (Canada Only) UDI-DI code: 00801741143243 *SureStep" Foley Tray System Bardex¿ IC Complete Care¿ REF: A300316A UDI code: 00801741073731 10801741073738 *SureStep" Foley Tray System Bardex¿ IC Complete Care¿ REF: A300318A UDI code: 00801741073748¿ 10801741073745 *SureStep" Foley Tray System Bardex¿ IC Complete Care¿ REF: A303314A A303316A A303318A UDI code: 00801741073786¿ 10801741073783 00801741073793¿ 10801741073790 00801741073809¿ 10801741073806 *SureStep" Foley Tray System Lubri-Sil¿ IC Complete Care¿ REF: A303414A UDI code: 00801741073816¿ 10801741073813 *(416A)SureStep" Foley Tray System Bardex¿ IC Complete Care¿ (714A/716A/718A)SureStep" Foley Tray System Bardex¿ IC Complete Care¿ (914)SureStep" Foley Tray System REF: A304716A A304714A A304716A A304718A UDI code: 00801741104206¿ 10801741104203 00801741104268 10801741104265 00801741104299¿ 10801741104296 00801741100376¿ 10801741100373 *SureStep" Foley Tray System Bardex¿ IC Complete Care¿ REF: A319416A UDI code: 00801741100307¿ 10801741100304 *SureStep…

Quantity: 212580

Distribution: Worldwide - U.S. Nationwide distribution including in the states of AK, AL, AR, AZ, CA, CO, CT, DE, FL, GA, HI, IA, ID, IL, IN, KS, KY, LA, MA, MD, ME, MI, MN, MO, MS, MT, NC, ND, NE, NH, NJ, NM, NV, NY, OH, OK, OR, PA, RI, SC, SD, TN, TX, UT, VA, WA, WI and WY. The countries of Bahrain, Canada, Costs Rica, Guatemala, Mexico, Saudi Arabia, and United Arab Emirates.

Recall number Z-3116-2026 in the FDA Enforcement Report. Check the lot numbers and dates on your product against the description above.

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Medical devices · Sep 16, 2026 · Class I · Ongoing

Bravo CF capsule delivery device, 5-pack, Product Number FGS-0635, Bravo CF capsule delivery device, 1-pack, Product Number FGS-0636. Used …

Given Imaging Ltd. · Yokne'Am Ilit, Israel

Why: Capsule may fail to attach to the esophagus or detach from the delivery device. Risks include patient aspiration/inhalation, perforation of esophagus, obstruction of the airway, hemorrhage/blood loss/bleeding, laceration of the esophagus, a delay in diagnosis, and foreign bodies remaining in the patient.

Product details, where it was sold and what to do

Bravo CF capsule delivery device, 5-pack, Product Number FGS-0635, Bravo CF capsule delivery device, 1-pack, Product Number FGS-0636. Used to attach a pH monitoring capsule to the esophagus.

Quantity: 127,416

Distribution: Worldwide distribution. US nationwide including Puerto Rico; Argentina, Australia, Austria, Bahrain, Brazil, Bulgaria, Canada, Cayman Islands, Chile, China, Czech Republic, Dominican Republic, France, Germany, Greece, Hong Kong, India, Ireland, Israel, Italy, Kazakhstan, Kenya, Luxembourg, Netherlands, New Zealand, Norway, Panama, Poland, Portugal, Singapore, South Africa, Spain, Sweden, Switzerland, Taiwan, Thailand, Trinidad And Tobago, United Arab Emirates, and United Kingdom.

Recall number Z-3090-2026 in the FDA Enforcement Report. Check the lot numbers and dates on your product against the description above.

Medical devices · Sep 16, 2026 · Class II · Ongoing

Citric Complete Dry Citric Acid Concentrate REF: DCA+200-25 & DCA+203-25

Nipro Renal Soultions USA, Corporation · Lewisberry, PA, United States

Why: Hemodialysis concentrates contain high endotoxin levels

Product details, where it was sold and what to do

Citric Complete Dry Citric Acid Concentrate REF: DCA+200-25 & DCA+203-25

Quantity: 7,770 cases

Distribution: Worldwide - US Nationwide distribution in the states of FL, GA, IL, MD, MI, NC, NJ, NV, OH, PA, and the countries of Guatemala and Panama.

Recall number Z-3135-2026 in the FDA Enforcement Report. Check the lot numbers and dates on your product against the description above.

Medical devices · Sep 16, 2026 · Class II · Ongoing

Products that contain the Pericare Wipes: SureStep Intermittent Catheter Tray REF: INTP16 INTS14 INTS14C INTS16 INTS16C PEDINTS06 PEDINTS08…

C.R. Bard Inc · Covington, GA, United States

Why: Due to complaints received indicating presence of contamination on the surface of pericare wipes provided with various Foley and Intermittent Catheter Trays.

Product details, where it was sold and what to do

Products that contain the Pericare Wipes: SureStep Intermittent Catheter Tray REF: INTP16 INTS14 INTS14C INTS16 INTS16C PEDINTS06 PEDINTS08 PEDINTS10 UDI code: 00801741183300¿ 10801741183307 00801741183218¿ 10801741183215 00801741183232 10801741183239 00801741183225¿ 10801741183222 00801741183249 10801741183246 00801741183263¿ 10801741183260 00801741183270¿ 10801741183277 00801741183287¿ 10801741183284 Preamendment REF: INTL14 INTL15 INTL16 INTP14 UDI code: 00801741183164¿ 10801741183161 00801741183171¿ 10801741183178 00801741183188 10801741183185 00801741183294 10801741183291 For urological use only, Intended for use in the drainage and/or collection and/or measurement of urine.

Quantity: 391720 units/kits

Distribution: Worldwide - U.S. Nationwide distribution including in the states of AK, AL, AR, AZ, CA, CO, CT, DE, FL, GA, HI, IA, ID, IL, IN, KS, KY, LA, MA, MD, ME, MI, MN, MO, MS, MT, NC, ND, NE, NH, NJ, NM, NV, NY, OH, OK, OR, PA, RI, SC, SD, TN, TX, UT, VA, WA, WI and WY. The countries of Bahrain, Canada, Costs Rica, Guatemala, Mexico, Saudi Arabia, and United Arab Emirates.

Recall number Z-3117-2026 in the FDA Enforcement Report. Check the lot numbers and dates on your product against the description above.

Medical devices · Sep 16, 2026 · Class I · Ongoing

Kit: Epidural/Pain TQC 20/Cs, REF: 82465 Containing Sodium Chloride Injection, 0.9%, USP 10ml ampules

Medical Action Industries, Inc. 306 · Arden, NC, United States

Why: Kits containing Sodium Chloride ampules subject to another recall are recalled due to potentially compromised sterility.

Product details, where it was sold and what to do

Kit: Epidural/Pain TQC 20/Cs, REF: 82465 Containing Sodium Chloride Injection, 0.9%, USP 10ml ampules

Quantity: 1,960

Distribution: US distribution to states of: IA, VA, MO, KS, FL, OH and LS.

Recall number Z-3106-2026 in the FDA Enforcement Report. Check the lot numbers and dates on your product against the description above.

Medical devices · Sep 16, 2026 · Class II · Ongoing

Halyard IV Start Kit Non-Sterile REF: KRIV26-02

AVID Medical, Inc. · Toano, VA, United States

Why: Convenience kits contain BD ChloraPrep Clear - 1 mL and FREPP Clear 1.5 mL Applicators which lacks sterility assurance due to to wrinkles in the paper lidding which may breach the seal area.

Product details, where it was sold and what to do

Halyard IV Start Kit Non-Sterile REF: KRIV26-02

Quantity: 98 Kits

Distribution: US Nationwide distribution in the state of NE.

Recall number Z-3109-2026 in the FDA Enforcement Report. Check the lot numbers and dates on your product against the description above.

Medical devices · Sep 16, 2026 · Class I · Ongoing

Kit: Single Shot Epidural 20/Cs, REF: 59553; Kit: Single Shot Epidural 20/Cs, REF: 83945B

Medical Action Industries, Inc. 306 · Arden, NC, United States

Why: Kits containing Sodium Chloride ampules subject to another recall are recalled due to potentially compromised sterility.

Product details, where it was sold and what to do

Kit: Single Shot Epidural 20/Cs, REF: 59553; Kit: Single Shot Epidural 20/Cs, REF: 83945B. Containing Sodium Chloride Injection, 0.9%, USP 10ml ampules

Quantity: 3,606

Distribution: US distribution to states of: IA, VA, MO, KS, FL, OH and LS.

Recall number Z-3107-2026 in the FDA Enforcement Report. Check the lot numbers and dates on your product against the description above.

Medical devices · Sep 16, 2026 · Class II · Ongoing

AMS Convenience Kit: DSAEK Pack - RX, Part Number AMS12394B

Windstone Medical Packaging, Inc. · Billings, MT, United States

Why: The convenience kits contain .0.9% Sodium Chloride Injection, USP products in Single Dose freeflex bags, which may contain blue Break-off-Parts (BOPs) that have detached from the infusion port during manipulation.

Product details, where it was sold and what to do

AMS Convenience Kit: DSAEK Pack - RX, Part Number AMS12394B

Quantity: 3,260 kits

Distribution: US Nationwide distribution in the states of CA, GA, WA.

Recall number Z-3138-2026 in the FDA Enforcement Report. Check the lot numbers and dates on your product against the description above.

Medical devices · Sep 16, 2026 · Class II · Ongoing

MedicaLyte Bicarbonate Powder REF: DB+201-2.1(45X) and DB+201-25 (35X, 36.83X, 45X))

Nipro Renal Soultions USA, Corporation · Lewisberry, PA, United States

Why: Hemodialysis concentrates contain high endotoxin levels

Product details, where it was sold and what to do

MedicaLyte Bicarbonate Powder REF: DB+201-2.1(45X) and DB+201-25 (35X, 36.83X, 45X))

Quantity: 2,327 cases

Distribution: Worldwide - US Nationwide distribution in the states of FL, GA, IL, MD, MI, NC, NJ, NV, OH, PA, and the countries of Guatemala and Panama.

Recall number Z-3134-2026 in the FDA Enforcement Report. Check the lot numbers and dates on your product against the description above.

Medical devices · Sep 16, 2026 · Class II · Ongoing

Products that contain the Pericare Wipes: (Canada Only) SureStep" Foley Tray System Bardex¿ IC Complete Care¿ REF: A300314AC UDI-DI code: 0…

C.R. Bard Inc · Covington, GA, United States

Why: Due to complaints received indicating presence of contamination on the surface of pericare wipes provided with various Foley and Intermittent Catheter Trays.

Product details, where it was sold and what to do

Products that contain the Pericare Wipes: (Canada Only) SureStep" Foley Tray System Bardex¿ IC Complete Care¿ REF: A300314AC UDI-DI code: 00801741143243 SureStep" Foley Tray System Bardex¿ IC Complete Care¿ REF: A300316AC UDI-DI code: 00801741143250 SureStep" Foley Tray System Lubri-Sil¿ IC Complete Care¿ REF: A319516AMC UDI-DI code: 00801741143472 SureStep" Foley Tray System Bard¿ Lubricath Foley REF: A800366C UDI-DI code: 00801741143571 SureStep" Foley Tray System Bard¿ Silicone Foley Catheter Tray REF: A897514C UDI-DI code: 00801741074011¿ SureStep" Foley Tray System Bard¿ Silicone Foley Catheter Tray REF: A897516C UDI-DI code: 00801741143595 SureStep" Foley Tray System Bard¿ Silicone Foley Catheter Tray REF: A902114C UDI-DI code: 00801741144325 ***** SureStep" Foley Tray System Lubri-Sil¿ IC Complete Care REF: A300416AC UDI code: 00801741143281 10801741143288 SureStep" Foley Tray System Bardex¿ IC Complete Care REF: A303314AC UDI code: 00801741143304 10801741143301 SureStep" Foley Tray System Lubri-Sil¿ IC Complete Care REF: A319514AMC UDI code: 00801741143465 10801741143462 SureStep" Foley Tray System Bard¿ Lubricath¿ Foley Catheter Tray REF: A800061C UDI code: 00801741144172 10801741144179 SureStep" Foley Tray System Bard¿ Lubricath¿ Foley Catheter Tray REF: A800065C UDI code: 00801741144202 10801741144209 SureStep" Foley Tray System Bard¿ Lubricath¿ Foley Catheter Tray REF: A800360C UDI code: 00801741143519 10801741143516 SureStep" Foley Tray System Bard…

Quantity: 364

Distribution: Worldwide - U.S. Nationwide distribution including in the states of AK, AL, AR, AZ, CA, CO, CT, DE, FL, GA, HI, IA, ID, IL, IN, KS, KY, LA, MA, MD, ME, MI, MN, MO, MS, MT, NC, ND, NE, NH, NJ, NM, NV, NY, OH, OK, OR, PA, RI, SC, SD, TN, TX, UT, VA, WA, WI and WY. The countries of Bahrain, Canada, Costs Rica, Guatemala, Mexico, Saudi Arabia, and United Arab Emirates.

Recall number Z-3119-2026 in the FDA Enforcement Report. Check the lot numbers and dates on your product against the description above.

Medical devices · Sep 16, 2026 · Class II · Ongoing

Citric Complete Liquid Citric Acid Concentrate REF: LC+200-D,LC+201, LC+225(45X)

Nipro Renal Soultions USA, Corporation · Lewisberry, PA, United States

Why: Hemodialysis concentrates contain high endotoxin levels

Product details, where it was sold and what to do

Citric Complete Liquid Citric Acid Concentrate REF: LC+200-D,LC+201, LC+225(45X)

Quantity: 100 drums/1072 cases

Distribution: Worldwide - US Nationwide distribution in the states of FL, GA, IL, MD, MI, NC, NJ, NV, OH, PA, and the countries of Guatemala and Panama.

Recall number Z-3136-2026 in the FDA Enforcement Report. Check the lot numbers and dates on your product against the description above.

Medical devices · Sep 16, 2026 · Class II · Ongoing

Getinge PVC Thoracic Catheter, Firm PVC Straight, 10 per Case

Atrium Medical Corporation · Merrimack, NH, United States

Why: An Out of Specification result (OOS) related to bacterial endotoxin testing in a single lot of catheters.

Product details, where it was sold and what to do

Getinge PVC Thoracic Catheter, Firm PVC Straight, 10 per Case; Size(Model Number): 1. 28FR(15028), 2. 36FR(15036);

Quantity: 256

Distribution: US Nationwide distribution.

Recall number Z-3113-2026 in the FDA Enforcement Report. Check the lot numbers and dates on your product against the description above.

Medical devices · Sep 16, 2026 · Class II · Ongoing

Products that contain the Pericare Wipes: Bardex Lubricath Foley Catheter Tray REF: 899914 899916 899918 UDI codes: 00801741024801¿ 1080174…

C.R. Bard Inc · Covington, GA, United States

Why: Due to complaints received indicating presence of contamination on the surface of pericare wipes provided with various Foley and Intermittent Catheter Trays.

Product details, where it was sold and what to do

Products that contain the Pericare Wipes: Bardex Lubricath Foley Catheter Tray REF: 899914 899916 899918 UDI codes: 00801741024801¿ 10801741024808 00801741024818¿ 10801741024815 00801741024825¿ 10801741024822 SureStep" Foley Tray System with Bardex¿ Lubricath Temp Sensing Foley Catheter REF: A119416M UDI code: 00801741073700 10801741073707 SureStep" Foley Tray System Bard¿ Lubricath Foley REF: A800361 UDI code: 00801741073939 10801741073936 SureStep" Foley Tray System Bard¿ Lubricath¿ Foley Catheter Tray REF: A899616 UDI code: 00801741104534¿ 10801741104531 SureStep" Foley Tray System Bardex¿ Lubricath¿ Foley Catheter REF: A899914 UDI code: 00801741074004 10801741074001 SureStep" Foley Tray System Bardex¿ Lubricath¿ Foley Catheter REF: A899916 UDI code: 00801741074011¿ 10801741074018 SureStep" Foley Tray System Bardex¿ Lubricath¿ Temperature Sensing Catheter REF: A900216 UDI code: 00801741120978¿ 10801741120975 SureStep" Foley Tray System Bard¿Lubricath¿ Foley Catheter REF: A902914 A902916 A902918 UDI code: 00801741074066¿10801741074063 00801741074073 10801741074070 00801741074080¿10801741074087 Bard¿ Urine Meter Foley Catheter Tray With Bardex¿ Lubricath¿ Foley Catheter REF: 304916 UDI code: 00801741019736 01801741019739 Bard¿ Urine Meter Foley Catheter Tray With Bardex¿ Lubricath¿ Foley Catheter REF: 902916 UDI codes: 00801741024863 10801741024860 (416A) SureStep Foley Tray System Bardex IC Complete Care (7…

Quantity: 12,463 trays/kits

Distribution: Worldwide - U.S. Nationwide distribution including in the states of AK, AL, AR, AZ, CA, CO, CT, DE, FL, GA, HI, IA, ID, IL, IN, KS, KY, LA, MA, MD, ME, MI, MN, MO, MS, MT, NC, ND, NE, NH, NJ, NM, NV, NY, OH, OK, OR, PA, RI, SC, SD, TN, TX, UT, VA, WA, WI and WY. The countries of Bahrain, Canada, Costs Rica, Guatemala, Mexico, Saudi Arabia, and United Arab Emirates.

Recall number Z-3114-2026 in the FDA Enforcement Report. Check the lot numbers and dates on your product against the description above.

Medical devices · Sep 16, 2026 · Class II · Ongoing

HeartSine SAM 350P 350P US Device, US English - 2 Min CPR UDI-DI codes: 0506016712067 350P US Device, US English (American Airlines) - 2 Mi…

HeartSine Technologies Ltd · Belfast, United Kingdom

Why: Due to a damaged (over stretched) membrane tail that causes an intermittent fault.

Product details, where it was sold and what to do

HeartSine SAM 350P 350P US Device, US English - 2 Min CPR UDI-DI codes: 0506016712067 350P US Device, US English (American Airlines) - 2 Min CPR UDI-DI code: 0506016712207 350P US Device, US English with Gateway - 2 Min CPR UDI-DI code: 0506016712804 HeartSine SAM 360P 360P US Device, US English - 2 Min CPR UDI-DI code: 0506016712068 HeartSine SAM 450P SAM 450P US Device, US English (2 min CPR) UDI-DI code: 0506016712069 The HeartSine samaritan¿ PAD (Public Access Defibrillator) Models SAM 350P, SAM 360P and SAM 450P are indicated for use on victims of cardiac arrest who are exhibiting the following signs: " Unconscious " Not breathing " Without circulation (without a pulse) The devices are indicated for use on patients greater than 8 years old or over 55 lbs. (25 kg) when used with the adult Pad-Pak (Pad-Pak-01 or Pad-Pak-07). They are indicated for use on children between 1 and 8 years of age or up to 55 lbs. (25 kg) when used with the Pediatric-Pad (Pad-Pak-02).

Quantity: 11,912

Distribution: Worldwide - U.S. Nationwide distribution including in the states of AK, AL, AZ, CA, CT, DC, FL, GA, HI, IA, ID, IL, IN, KS, KY, MA, MD, ME MI, MN, NC, NJ, NM, NV, NY, OH, OK, OR, PA, SD,TN, TX, UT, VA, WA, WI, WV and WY. The countries of Argentina, Australia, Brazil, Canada, Chile, Colombia, Hong Kong, Indonesia, ISRAEL, JAPAN, Malaysia, Netherlands, Philippines, POLAND, SINGAPORE, South Korea, Taiwan, Thailand and UNITED KINGDOM.

Recall number Z-3120-2026 in the FDA Enforcement Report. Check the lot numbers and dates on your product against the description above.

Medical devices · Sep 16, 2026 · Class II · Ongoing

Products that contain the Pericare Wipes: Bard¿ Foley Tray With Lubri-Sil¿ All-Silicone Foley Catheter REF: 947314 947316 947318 UDI codes:…

C.R. Bard Inc · Covington, GA, United States

Why: Due to complaints received indicating presence of contamination on the surface of pericare wipes provided with various Foley and Intermittent Catheter Trays.

Product details, where it was sold and what to do

Products that contain the Pericare Wipes: Bard¿ Foley Tray With Lubri-Sil¿ All-Silicone Foley Catheter REF: 947314 947316 947318 UDI codes: 00801741024924¿ 10801741024921 00801741024931¿ 10801741024938 00801741024948¿ 10801741024945 Lubri-Sil¿ I.C. Complete Care¿ All-Silicone Foley Catheter Tray REF: 300416A UDI code: 00801741024580 10801741024587 SureStep" Foley Tray System Lubri-Sil¿ IC Complete Care¿ REF: A300416A UDI code: 00801741073762¿ 10801741073769 SureStep" Foley Tray System Lubri-Sil¿ IC Complete Care REF: A303416A UDI code: 00801741073823 10801741073820 SureStep" Foley Tray System Lubri-Sil¿ IC Complete Care¿ REF: A307416A A307418A UDI codes: 00801741104381¿ 10801741104388 00801741100505¿ 10801741100502 SureStep" Foley Tray System Bard¿ Silicone Foley Catheter Tray REF: A897516 UDI code: 00801741073984 10801741073981 SureStep" Foley Tray System Bardex¿ All- Silicone Foley Catheter Tray REF: A902416 UDI code: 00801741074042¿ 10801741074049 SureStep" Foley Tray System Bardex¿ All- Silicone Foley Catheter Tray REF: A902418 UDI code: 00801741074059¿ 10801741074056 SureStep" Foley Tray System Bard¿ Lubri-Sil¿ Foley Catheter REF: A907316 UDI code: 00801741104749¿ 10801741104746 SureStep" Foley Tray System with Bard¿ Lubri-Sil¿ Catheter REF: A942210 UDI code: 00801741100567¿ 10801741100564 SureStep" Foley Tray System with Bard¿ Lubri-Sil¿ Catheter REF: A942212 UDI code: 00801741100536¿ 10801741100533 SureStep" Foley Tray System Bard¿ Lubri-Sil¿ Foley Ca…

Quantity: 283883 trays/kits

Distribution: Worldwide - U.S. Nationwide distribution including in the states of AK, AL, AR, AZ, CA, CO, CT, DE, FL, GA, HI, IA, ID, IL, IN, KS, KY, LA, MA, MD, ME, MI, MN, MO, MS, MT, NC, ND, NE, NH, NJ, NM, NV, NY, OH, OK, OR, PA, RI, SC, SD, TN, TX, UT, VA, WA, WI and WY. The countries of Bahrain, Canada, Costs Rica, Guatemala, Mexico, Saudi Arabia, and United Arab Emirates.

Recall number Z-3115-2026 in the FDA Enforcement Report. Check the lot numbers and dates on your product against the description above.

Medical devices · Sep 16, 2026 · Class II · Ongoing

Getinge PVC Thoracic Catheter, Soft PVC Straight, 10 per Case

Atrium Medical Corporation · Merrimack, NH, United States

Why: An Out of Specification result (OOS) related to bacterial endotoxin testing in a single lot of catheters.

Product details, where it was sold and what to do

Getinge PVC Thoracic Catheter, Soft PVC Straight, 10 per Case; Size(Model Number): 1. 16FR(8016), 2. 24FR(8024), 3. 28FR(8028), 4. 32FR(8032), 5. 36FR(8036);

Quantity: 3618

Distribution: US Nationwide distribution.

Recall number Z-3111-2026 in the FDA Enforcement Report. Check the lot numbers and dates on your product against the description above.

Medical devices · Sep 16, 2026 · Class II · Ongoing

Products that contain the Pericare Wipes: SureStep" Foley Tray System Add-A-Foley Catheter REF: A153200 UDI code: 00801741121067¿ 108017411…

C.R. Bard Inc · Covington, GA, United States

Why: Due to complaints received indicating presence of contamination on the surface of pericare wipes provided with various Foley and Intermittent Catheter Trays.

Product details, where it was sold and what to do

Products that contain the Pericare Wipes: SureStep" Foley Tray System Add-A-Foley Catheter REF: A153200 UDI code: 00801741121067¿ 10801741121064 SureStep" Foley Tray System Complete Care¿ Add-A-Foley Catheter REF: A304400A UDI code: 00801741073847¿ 10801741073844 SureStep" Foley Tray System Add-A-Foley Catheter REF: A399400 UDI code: 00801741100369¿ 10801741100366 SureStep" Foley Tray System Complete Care¿ Add-A-Foley Catheter REF: A399400A UDI code: 00801741073915¿ 10801741073912 SureStep" Foley Tray System Complete Care¿ Add-A-Foley Catheter REF: A904400A UDI code: 00801741074097¿ 10801741074094 SureStep Intermittent Catheter Tray REF: INTAAI UDI code: 00801741183317 10801741183314 For urological use only, Intended for use in the drainage and/or collection and/or measurement of urine.

Quantity: 33850 units/kits

Distribution: Worldwide - U.S. Nationwide distribution including in the states of AK, AL, AR, AZ, CA, CO, CT, DE, FL, GA, HI, IA, ID, IL, IN, KS, KY, LA, MA, MD, ME, MI, MN, MO, MS, MT, NC, ND, NE, NH, NJ, NM, NV, NY, OH, OK, OR, PA, RI, SC, SD, TN, TX, UT, VA, WA, WI and WY. The countries of Bahrain, Canada, Costs Rica, Guatemala, Mexico, Saudi Arabia, and United Arab Emirates.

Recall number Z-3118-2026 in the FDA Enforcement Report. Check the lot numbers and dates on your product against the description above.

Medical devices · Sep 16, 2026 · Class II · Ongoing

Product Name: DermaV Laser System Model/Catalog Number: DermaV Medical laser device that delivers pulsed laser energy at wavelengths of 532…

Lutronic Corporation · Goyang, Korea (the Republic of)

Why: Utilizing higher fluences at 1064nm wavelength with current cryogen parameters may result in a spark/loud noise during treatment, potentially resulting in patient burn.

Product details, where it was sold and what to do

Product Name: DermaV Laser System Model/Catalog Number: DermaV Medical laser device that delivers pulsed laser energy at wavelengths of 532 nm and 1064 nm through a fiber-optic handpiece. The system may be configured with an Intelligent Cooling Device (ICD) to provide epidermal cooling during laser treatment

Quantity: 1065

Distribution: Worldwide distribution - US Nationwide and the countries of Canada and European Union.

Recall number Z-3110-2026 in the FDA Enforcement Report. Check the lot numbers and dates on your product against the description above.

Medical devices · Sep 16, 2026 · Class II · Ongoing

MedicaLyte Liquid Bicarbonate Concentrate REF: BC-100 and BC+201

Nipro Renal Soultions USA, Corporation · Lewisberry, PA, United States

Why: Hemodialysis concentrates contain high endotoxin levels

Product details, where it was sold and what to do

MedicaLyte Liquid Bicarbonate Concentrate REF: BC-100 and BC+201

Quantity: 3,286 cases

Distribution: Worldwide - US Nationwide distribution in the states of FL, GA, IL, MD, MI, NC, NJ, NV, OH, PA, and the countries of Guatemala and Panama.

Recall number Z-3133-2026 in the FDA Enforcement Report. Check the lot numbers and dates on your product against the description above.

Medicines · Sep 16, 2026 · Class I · Ongoing

0.9% Sodium Chloride Injection, USP, 100 mL Partial Fill in 150 mL PAB Container, Sterile

B BRAUN MEDICAL INC · Allentown, PA, United States

Why: Presence of Particulate Matter: particulate matter identified as iron oxide, inorganic material, cellulose cotton fiber or polystyrene

Product details, where it was sold and what to do

0.9% Sodium Chloride Injection, USP, 100 mL Partial Fill in 150 mL PAB Container, Sterile, Rx only, B. Braun Medical Inc., Bethlehem, PA 18018 USA, NDC 0264-1800-32.

Quantity: 201,472 total container

Distribution: Nationwide within the United States

Recall number D-0869-2026 in the FDA Enforcement Report. Check the lot numbers and dates on your product against the description above.

Medicines · Sep 16, 2026 · Class I · Ongoing

Dextrose Injection, USP, 70 %, 2000 mL bags

Baxter Healthcare Corporation · Deerfield, IL, United States

Why: Presence of Particulate Matter: particulate matter identified as stainless steel particles in the solution.

Product details, where it was sold and what to do

Dextrose Injection, USP, 70 %, 2000 mL bags, Rx Only, Baxter Healthcare Corporation Deerfield, IL, 60016, Made in USA, NDC 00338-0719-06

Quantity: 606 bags

Distribution: U.S. Nationwide.

Recall number D-0850-2026 in the FDA Enforcement Report. Check the lot numbers and dates on your product against the description above.

What to do if you own a recalled product

  1. Match it exactly. Recalls usually cover specific lot or batch numbers, "best by" dates, model numbers or sizes. Compare every detail on your product with the notice.
  2. Stop using it. For food and medicine, do not eat, take or give it to pets, even if it looks and smells fine: Listeria and Salmonella do not change how food looks.
  3. Follow the remedy. Most recalls offer a refund, repair or replacement. Return food to the store or follow the company's instructions; for products, contact the company named in the notice.
  4. Do not stop a prescription medicine on your own. Ask your pharmacist or doctor first. They can swap you to an unaffected batch.
  5. Report problems. In the U.S., report illnesses from food or medicine to FDA MedWatch and injuries from products to SaferProducts.gov.

Beware of recall scams

Criminals send fake "recall refund" texts and emails that ask you to pay a "shipping fee" or enter card details. Real recalls never ask for payment. Paste any suspicious recall message into our scam text checker. Read more: Product recalls: how they work and what to do.

Sources: U.S. Food and Drug Administration Enforcement Reports (via openFDA) and the U.S. Consumer Product Safety Commission recall database. FDA enforcement reports list recalls when they are classified, which can be a few weeks after the company's first announcement. Vehicle recalls are available per vehicle in our VIN check.