Updated 7 hours ago · U.S. FDA & CPSC

Recalls today

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.

Counts are for the last 30 days.

Advertisement

Latest recalls

Food · Oct 28, 2026 · Class III · Ongoing

Textured Soy Protein

El Ruisenor De Mexico, Inc. · Vernon, CA, United States

Why: undeclared allergen ingredient (Soy)

Product details, where it was sold and what to do

Textured Soy Protein; packaged in 1lb, 5lb, 33lb clear plastic units. No UPC

Quantity: 123.5 pounds

Distribution: Recalling firm distributes primarily to California customers both retail and wholesale. Additional distribution to limited customers in Hawaii, Illinois, Kansas, Nevada, Oregon, and Washington.

Recall number H-0155-2027 in the FDA Enforcement Report. Check the lot numbers and dates on your product against the description above.

Food · Oct 28, 2026 · Class III · Ongoing

10X10 Wheat Snack

El Ruisenor De Mexico, Inc. · Vernon, CA, United States

Why: undeclared allergen ingredient (Wheat)

Product details, where it was sold and what to do

10X10 Wheat Snack; packaged in 2lb, 5lb, 33lb clear plastic units. No UPC

Quantity: 942 pounds

Distribution: Recalling firm distributes primarily to California customers both retail and wholesale. Additional distribution to limited customers in Hawaii, Illinois, Kansas, Nevada, Oregon, and Washington.

Recall number H-0159-2027 in the FDA Enforcement Report. Check the lot numbers and dates on your product against the description above.

Food · Oct 28, 2026 · Class III · Ongoing

Black Sesame Seeds

El Ruisenor De Mexico, Inc. · Vernon, CA, United States

Why: undeclared allergen ingredient (Sesame)

Product details, where it was sold and what to do

Black Sesame Seeds; packed in a clear plastic bag. 1lb, 5lb, 50lb unit size. No UPC

Quantity: 156.97 pounds

Distribution: Recalling firm distributes primarily to California customers both retail and wholesale. Additional distribution to limited customers in Hawaii, Illinois, Kansas, Nevada, Oregon, and Washington.

Recall number H-0104-2027 in the FDA Enforcement Report. Check the lot numbers and dates on your product against the description above.

Food · Oct 28, 2026 · Class II · Ongoing

Fritura mixed dry fruit

El Ruisenor De Mexico, Inc. · Vernon, CA, United States

Why: undeclared allergen ingredient (Wheat, Yellow #5, Yellow #6)

Product details, where it was sold and what to do

Fritura mixed dry fruit; packed in a clear plastic 1lb, 5lb, 25lb unit sizes. no UPC

Quantity: 134.59 pounds

Distribution: Recalling firm distributes primarily to California customers both retail and wholesale. Additional distribution to limited customers in Hawaii, Illinois, Kansas, Nevada, Oregon, and Washington.

Recall number H-0120-2027 in the FDA Enforcement Report. Check the lot numbers and dates on your product against the description above.

Food · Oct 28, 2026 · Class I · Ongoing

Special Red Almond Mole Powder

El Ruisenor De Mexico, Inc. · Vernon, CA, United States

Why: undeclared allergen ingredient (Sesame, Peanuts, Wheat, Soy, Almonds, Walnuts, Yellow#5, Yellow#6, Red#40, Blue#2)

Product details, where it was sold and what to do

Special Red Almond Mole Powder; packaged in 1lb, 5lb, 11lb clear plastic units. No UPC

Quantity: 1,277.91 pounds

Distribution: Recalling firm distributes primarily to California customers both retail and wholesale. Additional distribution to limited customers in Hawaii, Illinois, Kansas, Nevada, Oregon, and Washington.

Recall number H-0141-2027 in the FDA Enforcement Report. Check the lot numbers and dates on your product against the description above.

Food · Oct 28, 2026 · Class III · Ongoing

Whole wheat flour

El Ruisenor De Mexico, Inc. · Vernon, CA, United States

Why: undeclared allergen ingredient (Wheat)

Product details, where it was sold and what to do

Whole wheat flour; packaged in 1lb, 5lb, 50lb clear plastic units. No UPC

Quantity: 237 pounds

Distribution: Recalling firm distributes primarily to California customers both retail and wholesale. Additional distribution to limited customers in Hawaii, Illinois, Kansas, Nevada, Oregon, and Washington.

Recall number H-0162-2027 in the FDA Enforcement Report. Check the lot numbers and dates on your product against the description above.

Food · Oct 28, 2026 · Class II · Ongoing

Milk Chocolate Covered Raisins

El Ruisenor De Mexico, Inc. · Vernon, CA, United States

Why: undeclared allergen ingredient (Milk, Soy)

Product details, where it was sold and what to do

Milk Chocolate Covered Raisins; packaged in 1lb, 5lb, 20lb clear plastic units. No UPC

Quantity: 61.37 pounds

Distribution: Recalling firm distributes primarily to California customers both retail and wholesale. Additional distribution to limited customers in Hawaii, Illinois, Kansas, Nevada, Oregon, and Washington.

Recall number H-0158-2027 in the FDA Enforcement Report. Check the lot numbers and dates on your product against the description above.

Food · Oct 28, 2026 · Class II · Ongoing

Jovy Gummy Worms Neon

El Ruisenor De Mexico, Inc. · Vernon, CA, United States

Why: undeclared allergen ingredient (Red#40, Yellow#5, Yellow#6, Blue#1)

Product details, where it was sold and what to do

Jovy Gummy Worms Neon; packaged in 1lb plastic units. UPC 712199083411

Quantity: 521 pounds

Distribution: Recalling firm distributes primarily to California customers both retail and wholesale. Additional distribution to limited customers in Hawaii, Illinois, Kansas, Nevada, Oregon, and Washington.

Recall number H-0130-2027 in the FDA Enforcement Report. Check the lot numbers and dates on your product against the description above.

Consumer products · Oct 22, 2026

VQQQ Gas Patio Heaters Recalled Due to Risk of Serious Injury or Death from Fire and Burn Hazards

· China

Why: Components on the recalled patio heaters can malfunction, causing gas to be released, posing a risk of serious injury or death from fire and burn hazards.

Product details, where it was sold and what to do

VQQQ Natural Gas Patio Heaters. This recall involves VQQQ-branded natural gas patio heaters, models VQQQ-A1 and VQQQ-001. They have a bronze pole with a round base and a silver mushroom-shaped top with an adjustable height of 55 inches to 78 inches. A 24-foot-long gray gas hose is attached to the heater's base. The brand and model numbers are printed on the product's purchase receipt.

Quantity: About 100

Distribution: Sold at Sold Online At: Amazon.com from July 2024 through August 2026 for about $346., Shanxi Yuhe Sheng Maoyi Youxian Gongsi, dba VQQQ, of China

Remedy: Consumers should stop using the recalled patio heaters immediately, shut the valve at the portable gas source, disconnect the gas hose and contact VQQQ for a full refund. Consumers will be asked to write in permanent marker "Recalled" on the heater's base and send a photo of the marked heater to vqqqrecall@163.com. Consumers should then dispose of the recalled product.

Official CPSC recall notice ↗

Consumer products · Oct 22, 2026

Lithonia Lighting Recalls RSX Luminaires with Adjustable Tilt Arm Mountings Due to Risk of Serious Injury from Impact Hazard

Lithonia Lighting, of Atlanta, Georgia · United States, Mexico

Why: The knuckle of the recalled adjustable tilt arm mountings can fail, allowing the luminaire to fall from the mounting arm, posing a risk of serious injury due to impact hazard.

Product details, where it was sold and what to do

Lithonia Lighting RSX Luminaires with AASP, AARP, AAWB, and AAWSC Adjustable Tilt Arm Mountings used for commercial outdoor lighting.. This recall involves Luminaires with certain adjustable tilt mounting arms manufactured between August 2019 to July 2020 and August 2024 to April 2026: AASP, AARP, AAWB, and AAWSC. The adjustable tilt arm mounts the RSX luminaire to a square pole, round pole, wall bracket or wall bracket with surface mount conduit. The arm mount allows the luminaire to be tilted from 0 degrees to 90 degrees above horizontal. Consumers should contact Lithonia Lighting to confirm their Luminaire with adjustable tilt mounting arms are included in the recall.

Quantity: About 11,532

Distribution: Sold at Sold At: Commercial distributors nationwide including Turtle & Hughes Inc. and Consolidated Electrical Distributors for commercial outdoor lighting applications from August 2019 to August 2026 for between $400 and $2200.

Remedy: Consumers should keep clear of the area directly beneath the Luminaire and contact Lithonia Lighting to schedule a free repair. Lithonia Lighting will arrange for a qualified professional to replace the recalled adjustable tilt arm mount with a new complete adjustable arm assembly.

Official CPSC recall notice ↗

Advertisement
Consumer products · Oct 22, 2026

FoShanShiNanHaiQuNuoAiTongZhuangShangHang Recalls CIYTI Light-Up Princess Costumes Due to Risk of Serious Injury or Death from Battery Ingestion; Violate Mandatory Standard for Toys

· China

Why: The costumes violate the mandatory safety standard for toys because the button cell batteries can be accessed easily by children, posing a deadly ingestion hazard. If button cell or coin batteries are swallowed, the ingested batteries can cause serious injuries, including internal chemical burns, and death.

Product details, where it was sold and what to do

CIYTI Light-Up Princess Costumes. This recall involves CIYTI Light-Up Princess Costumes. The costumes include a blue dress with a crown and wand that light up, and a remote control. The crowns, scepters, and remote controls contain button batteries. There are no markings on the product. The package has "CIYTI" on the front.

Quantity: About 94

Distribution: Sold at Sold Online At: Amazon from February 2025 through June 2025 for between $21 and $35., FoShanShiNanHaiQuNuoAiTongZhuangShangHang, of China

Remedy: Consumers should take the princess costumes away from children immediately, stop using them and contact FoShanShiNanHaiQuNuoAiTongZhuangShangHang for a full refund. Consumers will be asked to write "RECALLED" with permanent marker on the dress, crown, wand, and remote, then throw away the toys and submit a photo of the disposed toys to Norakid2026@outlook.com. Note: Button cell batteries are hazar

Official CPSC recall notice ↗

Consumer products · Oct 22, 2026

Costway Recalls Convertible High Chairs Due to Risk of Serious Injury or Death from Entrapment and Fall Hazards; Violate Mandatory Standard for High Chairs

· China

Why: The convertible high chairs violate the mandatory safety standard for high chairs because they do not contain a passive restraint system and a child can slip through the opening between the feeding tray and seat and become entrapped or fall, posing a risk of serious injury or death.

Product details, where it was sold and what to do

Costway Convertible High Chairs. This recall involves Costway high chairs designed to convert into a table and chair set. They were available in several color combinations, including purple and white, red and white, blue and white, and brown and white. There is no tracking information located on the products.

Quantity: About 3,332

Distribution: Sold at Sold At: Walmart and Target stores nationwide and online at Costway.com from May 2023 through July 2026 for between $84 and $100., Goplus Corporation, dba Costway, of Fontana, California

Remedy: Consumers should immediately stop using the recalled high chairs and contact Costway for a free replacement high chair. Consumers will be asked to provide a receipt or a photo of the product and will receive a prepaid label to return the recalled product to Costway. Upon receipt of the recalled product, Costway will ship a replacement high chair free of charge.

Official CPSC recall notice ↗

Consumer products · Oct 22, 2026

BAMAMON Recalls LED Projecting Finger Light Toys Due to Risk of Serious Injury or Death from Battery Ingestion; Violate Mandatory Standard for Toys

· China

Why: None reported.

Product details, where it was sold and what to do

Bamamon LED Projecting Finger Light Toys. This recall involves Bamamon LED Projecting Finger Light toys which contain three button cells batteries. The finger lights come in 32 pieces in a box in red, orange, blue, black, purple, clear, green and yellow. The finger lights project eight space themed patterns such as astronauts, rockets, UFO, galaxy and solar systems printed on labels located on the front of the package.

Quantity: About 6,533

Distribution: Sold at Sold At: Amazon.com from March 2025 through August 2026 for about $13 to $14., Shenzhen Maiduoduo Trading Technology Co., Ltd., dba Bamamon, of China

Remedy: Consumers should stop using the toys immediately and contact Bamamon. Consumers will be asked to email a photograph showing the product being properly disposed of in the trash to bamamonproductrecall@outlook.com.

Official CPSC recall notice ↗

Medical devices · Oct 21, 2026 · Class II · Ongoing

RAPICIDE PA Part A High-Level Disinfectant, Model/Catalog Number: ML020116

Steris Corporation · Mentor, OH, United States

Why: If the vented cap becomes blocked, gas may accumulate and the bottle may swell due to increased internal pressure. In some cases, excess vapor or liquid chemistry may escape from the bottle when the cap is twisted during opening, which could result in user exposure if required personal protective equipment (PPE) is not properly used. Such exposure may result in injury to the user or others in close proximity.

Product details, where it was sold and what to do

RAPICIDE PA Part A High-Level Disinfectant, Model/Catalog Number: ML020116

Quantity: 11806 units

Distribution: Worldwide - US Nationwide distribution.

Recall number Z-0155-2027 in the FDA Enforcement Report. Check the lot numbers and dates on your product against the description above.

Medical devices · Oct 21, 2026 · Class II · Ongoing

NeuroStar Advanced Therapy System

Neuronetics, Inc. · Malvern, PA, United States

Why: Cables are not in conformance with the product specifications required in the production of the HP Coil Assembly.

Product details, where it was sold and what to do

NeuroStar Advanced Therapy System. Contains the NeuroStar HP Coil Assembly Part Number 81-01000-200. Affects the below NeuroStar Advanced Therapy Systems: 1. NeuroStar 2.0 US; Part Number: 81-01315-000. 2. NeuroStar 3.0 US; Part Number: 81-02315-000. 3. NeuroStar 2.X to 3.2 Upgrade Kit; Part Number: 81-25000-100. 4. NeuroStar Upgrade Kit 3.0 US; Part Number: 81-35000-000. 5. NeuroStar Mobile Console 3.6, 120V, US; Part Number: 81-03315-000. 6. NeuroStar Mobile Console 3.7, 120V, US; Part Number: 81-04315-000. 7. NeuroStar Mobile Console 3.8, 120V, US; Part Number: 81-05315-000.

Quantity: 179 units

Distribution: Worldwide distribution - US Nationwide and the countries of Japan and South Korea.

Recall number Z-0142-2027 in the FDA Enforcement Report. Check the lot numbers and dates on your product against the description above.

Medical devices · Oct 21, 2026 · Class II · Ongoing

Medline surgical convenience kits labeled as: 1) EAR, Medline product number/SKU DYNJ909020B

Medline Industries, LP · Northfield, IL, United States

Why: Medical convenience kits were distributed containing cannula components which do not conform to ISO 80369-7 dimensional requirements and may contribute to leaking or breaking during use.

Product details, where it was sold and what to do

Medline surgical convenience kits labeled as: 1) EAR, Medline product number/SKU DYNJ909020B; 2) EAR, Medline product number/SKU DYNJ909020A; 3) CAROTID PACK, Medline product number/SKU DYNJ42922C; 4) EAR, Medline product number/SKU DYNJ909020; 5) FEM CAROTID PACK, Medline product number/SKU DYNJ65706; 6) CAROTID CDS-LF, Medline product number/SKU CDS983139B.

Quantity: 620 kits

Distribution: US Nationwide distribution.

Recall number Z-0173-2027 in the FDA Enforcement Report. Check the lot numbers and dates on your product against the description above.

Medical devices · Oct 21, 2026 · Class II · Ongoing

NaviFlex LW Pusher

Boston Scientific Corporation · Marlborough, MA, United States

Why: Device was incorrectly manufactured with a guidewire exit port (referred to in the IFU as the RX port), which is not a design feature associated with this device configuration.

Product details, where it was sold and what to do

NaviFlex LW Pusher; Advx Panc. Stent 4/5F; Material Number (UPN): M00535030;

Quantity: 403

Distribution: US Nationwide distribution in the states of AL, CA, FL, GA, IL, IN, KY, MD, NC, NH, NM, NY, RI, TX, WA, WI, WV and the countries in TBD.

Recall number Z-0143-2027 in the FDA Enforcement Report. Check the lot numbers and dates on your product against the description above.

Medical devices · Oct 21, 2026 · Class II · Ongoing

Generic Name: FilmArray¿ Pneumonia Panel Generic Name: FilmArray¿ Pneumonia Panel Model/Catalog Number: RFIT-ASY-0144 (30 pack), RFIT-ASY-0…

BioFire Diagnostics, LLC · Salt Lake City, UT, United States

Why: Due to potential contaiminated of spefic lots of pneumonia and joint infection panels that could result in false positive results

Product details, where it was sold and what to do

Generic Name: FilmArray¿ Pneumonia Panel Generic Name: FilmArray¿ Pneumonia Panel Model/Catalog Number: RFIT-ASY-0144 (30 pack), RFIT-ASY-0145 (6 pack), FLM1-ASY-0150 (Verification Kits). Verification kit lots (FLM1-ASY-0150) are a sales configuration that consume kits from panel lots (RFIT-ASY-0144). Software Version: N/A Product Description: Multiple-type respiratory pathogen nucleic acid IVD, kit, nucleic acid technique (NAT) Component: N/A

Quantity: 4,892

Distribution: Worldwide - U.S. Nationwide distribution including in the states and territory of AK, AL, AR, AZ, CA, CO, CT, DC, FL, GA, GU, HI, IA, ID, IL, IN, KS, KY, LA, MA, MD, MI, MN, MO, MS, MT, NC, ND, NE, NJ, NM, NV, NY, OH, OK, OR, PA, PR, SC, SD, TN, TX, UT, VA, WA, WI, WV, and WY. The countries of United Arab Emirates, Netherland Antilles, Argentina, Austria, Bosnia and Herzegovina, Belgium, Bulgaria, Bolivia, Canada, Switzerland, Chile, China, Colombia, Costa Rica, Czech Republic, Germany, Denmark, Dominican Republic, Algeria, Ecuador, Spain, Finland, France, United Kingdom, Greece, Guatemala, H…

Recall number Z-0148-2027 in the FDA Enforcement Report. Check the lot numbers and dates on your product against the description above.

Medical devices · Oct 21, 2026 · Class II · Ongoing

TS Misc

Howmedica Osteonics Corp. · Mahwah, NJ, United States

Why: Reprocessing instructions provided in LSTPI-B specify a sterilization dry time of 30 minutes for the trays sterilized in blue wrap. When blue wrap is used, the 30-minute dry time may lead to a small amount of residual moisture remaining after sterilization.

Product details, where it was sold and what to do

TS Misc. Instruments Tray, Triathlon. Catalog Number: 6543-6-519.

Quantity: 577 trays

Distribution: These trays are provided by sale or loan. Loans are provided through Distributor. Foreign Consignees will be identified by the countries impacted. 158 trays have been distributed OUS.

Recall number Z-0167-2027 in the FDA Enforcement Report. Check the lot numbers and dates on your product against the description above.

Medical devices · Oct 21, 2026 · Class II · Ongoing

BD Phoenix Panel NMIC-306. Catalog Number: 449292.

Becton Dickinson & Co. · Sparks, MD, United States

Why: Potential for quality control failures with Klebsiella pneumoniae ATCC BAA-1705 when using the CPO Ambler classification feature.

Product details, where it was sold and what to do

BD Phoenix Panel NMIC-306. Catalog Number: 449292.

Quantity: 669,200 units

Distribution: US Nationwide distribution.

Recall number Z-0140-2027 in the FDA Enforcement Report. Check the lot numbers and dates on your product against the description above.

Medical devices · Oct 21, 2026 · Class II · Ongoing

JenaValve Trilogy Delivery Catheter, Size 23MM REF: TRILOGY-DC-S

Jenavalve Technology Inc. · Irvine, CA, United States

Why: Delivery Catheter may have sleeve liner separation that results in difficulty or inability to deploy heart valve device.

Product details, where it was sold and what to do

JenaValve Trilogy Delivery Catheter, Size 23MM REF: TRILOGY-DC-S

Quantity: 111 units

Distribution: US Nationwide distribution in the states of AZ, CA, FL, GA, IL, MA, MD, MI, MN, MO, NY, OH, PA, SC, TX, UT, VA, WA and the countries of Germany, Denmark, Great Britain, Italy.

Recall number Z-0134-2027 in the FDA Enforcement Report. Check the lot numbers and dates on your product against the description above.

Medical devices · Oct 21, 2026 · Class II · Ongoing

Convenience Kits containing CONMED AirSeal Access Ports ADVANCE LAPAROSCOPIC DYNJ911135 LAP CHOLE DYNJ911660 LAP NISSEN DYNJ911560 UROLOGY …

Medline Industries, LP · Northfield, IL, United States

Why: Kits contain CONMED AirSeal Access Ports. The ports were recalled by manufacturer due to potential for erroneous overpressure alerts and system venting during use, which may result in delays or ending procedures.

Product details, where it was sold and what to do

Convenience Kits containing CONMED AirSeal Access Ports ADVANCE LAPAROSCOPIC DYNJ911135 LAP CHOLE DYNJ911660 LAP NISSEN DYNJ911560 UROLOGY LAPAROSCOPIC - 51638 DYNJ908720A

Quantity: 3,551 kits

Distribution: US Nationwide distribution in the states of AZ, CA, IN, MD, MO, NJ, OH, and WI.

Recall number Z-0180-2027 in the FDA Enforcement Report. Check the lot numbers and dates on your product against the description above.

Medical devices · Oct 21, 2026 · Class II · Ongoing

Medline surgical convenience kits labeled as: CABG AUXILIARY PACK, Medline Product Number/SKU DYNJ44925D

Medline Industries, LP · Northfield, IL, United States

Why: Medical convenience kits were distributed containing cannula components which do not conform to ISO 80369-7 dimensional requirements and may contribute to leaking or breaking during use.

Product details, where it was sold and what to do

Medline surgical convenience kits labeled as: CABG AUXILIARY PACK, Medline Product Number/SKU DYNJ44925D

Quantity: 3125 kits

Distribution: US Nationwide distribution.

Recall number Z-0168-2027 in the FDA Enforcement Report. Check the lot numbers and dates on your product against the description above.

Medical devices · Oct 21, 2026 · Class II · Ongoing

Scout MD, REF MDS05A-01, MDS05C-01, MDS10C-01 Contents: (1) Scout MD Delivery System, Standard for use with the SCOUT MD Surgical Guidance …

Merit Medical Systems, Inc. · South Jordan, UT, United States

Why: The implantable clip may experience difficulties deploying, which could prevent the reflector from functioning as intended during use.

Product details, where it was sold and what to do

Scout MD, REF MDS05A-01, MDS05C-01, MDS10C-01 Contents: (1) Scout MD Delivery System, Standard for use with the SCOUT MD Surgical Guidance System, Rx Only, Sterile-EO

Distribution: US: AZ, CA, FL, IN, LA, NV, RI OUS: None

Recall number Z-0187-2027 in the FDA Enforcement Report. Check the lot numbers and dates on your product against the description above.

Medical devices · Oct 21, 2026 · Class II · Ongoing

Vinyl Instrument Guards, labeled as: 1) VENTED INSTRUMENT GUARD 1/16 X 3/4H - WHITE, Model Number 09-1-011; 2) WHITE VENTED INSTRUMENT GUAR…

Healthmark Industries Co., Inc. · Fraser, MI, United States

Why: Labeling not compliant with 21 CFR 801 and steam sterilization IFU has been updated.

Product details, where it was sold and what to do

Vinyl Instrument Guards, labeled as: 1) VENTED INSTRUMENT GUARD 1/16 X 3/4H - WHITE, Model Number 09-1-011; 2) WHITE VENTED INSTRUMENT GUARD 1/16 X 3/4, Model Number 09-1-011; 3) VENTED INSTRUMENT GUARD 5/64 X 3/4 - BLUE, Model Number 09-1-012; 4) BLUE VENTED INSTRUMENT GUARD 5/64 X 3/4, Model Number 09-1-012; 5) VENTED INSTRUMENT GUARD 7/64 X 3/4 - GREEN, Model Number 09-1-013; 6) GREEN VENTED INSTRUMENT GUARD 7/64 X 3/4, Model Number 09-1-013; 7) VENTED INSTRUMENT GUARD 1/8 X 1 - RED, Model Number 09-1-014; 8) RED VENTED INSTRUMENT GUARD 1/8 X 1, Model Number 09-1-014; 9) VENTED INSTRUMENT GUARD 3/16 X 1 - YELLOW, Model Number 09-1-015; 10) YELLOW VENTED INSTRUMENT GUARD 3/16 X 1, Model Number 09-1-015; 11) VENTED INSTRUMENT GUARD 13/32 X 3/4 - MAROON, Model Number 09-1-016; 12) MAROON VENTED INSTRUMENT GUARD 13/32 X 3/4, Model Number 09-1-016; 13) MAROON VENTED INSTRU GUARD 13/32 X 3/4, Model Number 09-1-016; 14) VENTED INSTRUMENT GUARD 1/16 X 3/8 X 1 - ORANGE, Model Number 09-1-017; 15) ORANGE VENTED INSTRUMENT GUARD 1/16 X 3/8 X 1, Model Number 09-1-017; 16) OR VENTED INSTRU GUARD 1/16 X 3/8 X 1, Model Number 09-1-017; 17) VENTED INSTRUMENT GUARD 5/64 X 5/8 X 1 - BROWN, Model Number 09-1-018; 18) BROWN VENTED INSTRUMENT GUARD 5/64 X 5/8 X 1, Model Number 09-1-018; 19) BROWN VENTED INSTRU GUARD 5/64 X 5/8 X 1, Model Number 09-1-018; 20) VENTED INSTRUMENT GUARD 1/8 X 1 X 1 - BLACK, Model Number 09-1-019; 21) BLACK VENTED INSTRUMENT GUARD 1/8 X 1 X 1, Model Number 09-1-019…

Quantity: 12,835,920 units

Distribution: Worldwide distribution - US Nationwide and the countries of JAPAN, AUSTRALIA, CANADA, PORTUGAL, FRANCE, POLAND, PUERTO RICO, SAUDI ARABIA, HONG KONG, BAHRAIN, QATAR, OMAN, ISRAEL, MEXICO, UNITED ARAB EMIRATES, SINGAPORE, BERMUDA, SOUTH KOREA, THAILAND, and UNITED KINGDOM.

Recall number Z-0188-2027 in the FDA Enforcement Report. Check the lot numbers and dates on your product against the description above.

Medical devices · Oct 21, 2026 · Class II · Ongoing

BD Phoenix Panel NMIC-312. Catalog Number: 449082.

Becton Dickinson & Co. · Sparks, MD, United States

Why: Potential for quality control failures with Klebsiella pneumoniae ATCC BAA-1705 when using the CPO Ambler classification feature.

Product details, where it was sold and what to do

BD Phoenix Panel NMIC-312. Catalog Number: 449082.

Quantity: 553,625 units

Distribution: US Nationwide distribution.

Recall number Z-0139-2027 in the FDA Enforcement Report. Check the lot numbers and dates on your product against the description above.

Medical devices · Oct 21, 2026 · Class II · Ongoing

Convenience Kits containing CONMED AirSeal Access Ports HERNANDEZ DAVINCI ACC BUNDLE M DYNJ911258 KIT ROBOTICS UROLOGY PROSTATE DYKMBNDL116…

Medline Industries, LP · Northfield, IL, United States

Why: Kits contain CONMED AirSeal Access Ports. The ports were recalled by manufacturer due to potential for erroneous overpressure alerts and system venting during use, which may result in delays or ending procedures.

Product details, where it was sold and what to do

Convenience Kits containing CONMED AirSeal Access Ports HERNANDEZ DAVINCI ACC BUNDLE M DYNJ911258 KIT ROBOTICS UROLOGY PROSTATE DYKMBNDL116I ROBOTIC CHEST DYNJ910997 DYNJ910997A RR-DAVINCI PROSTATE ACCESSORY DYNJ63392D UROLOGY LAPAROSCOPIC - 51638 DYNJ908720B UROLOGY ROBOT ADD ON PACK DYNJ85189

Quantity: 3,551 kits

Distribution: US Nationwide distribution in the states of AZ, CA, IN, MD, MO, NJ, OH, and WI.

Recall number Z-0181-2027 in the FDA Enforcement Report. Check the lot numbers and dates on your product against the description above.

Medical devices · Oct 21, 2026 · Class II · Ongoing

Curaplex Capnography EtCO2/O2 Oral/Nasal Cannula Multipack (10 pk), Item Number 670272-KIT

Sarnova HC, Llc · Dublin, OH, United States

Why: Affected kits were assembled with pediatric nasal cannula instead of the intended adult nasal cannula.

Product details, where it was sold and what to do

Curaplex Capnography EtCO2/O2 Oral/Nasal Cannula Multipack (10 pk), Item Number 670272-KIT

Quantity: 2,500 kits

Distribution: US Nationwide distribution in the states of IA, IL, IN, KY, MI, MN, MO, ND, OH, UT.

Recall number Z-0144-2027 in the FDA Enforcement Report. Check the lot numbers and dates on your product against the description above.

Medical devices · Oct 21, 2026 · Class II · Ongoing

Convenience Kits containing CONMED AirSeal Access Ports GENERAL DAVINCI DYNJG901004C LAP CHOLE DYNJ88071 ROBOTIC PACK DYNJ50474F

Medline Industries, LP · Northfield, IL, United States

Why: Kits contain CONMED AirSeal Access Ports. The ports were recalled by manufacturer due to potential for erroneous overpressure alerts and system venting during use, which may result in delays or ending procedures.

Product details, where it was sold and what to do

Convenience Kits containing CONMED AirSeal Access Ports GENERAL DAVINCI DYNJG901004C LAP CHOLE DYNJ88071 ROBOTIC PACK DYNJ50474F

Quantity: 3,551 kits

Distribution: US Nationwide distribution in the states of AZ, CA, IN, MD, MO, NJ, OH, and WI.

Recall number Z-0182-2027 in the FDA Enforcement Report. Check the lot numbers and dates on your product against the description above.

Medical devices · Oct 21, 2026 · Class II · Ongoing

1) Product Name AUD OPEN HEART PACK, Medline Kit Number/SKU DYNJ22052I

Medline Industries, LP · Northfield, IL, United States

Why: Medical convenience kits were distributed containing cannula components which do not conform to ISO 80369-7 dimensional requirements and may contribute to leaking or breaking during use.

Product details, where it was sold and what to do

1) Product Name AUD OPEN HEART PACK, Medline Kit Number/SKU DYNJ22052I; 2) Product Name AV SHUNT PACK-MARYVIEW, Medline Kit Number/SKU DYNJ24528N; 3) Product Name AV SHUNT PACK-MARYVIEW, Medline Kit Number/SKU DYNJ24528O; 4) Product Name AV SHUNT PACK-MARYVIEW, Medline Kit Number/SKU DYNJ24528P; 5) Product Name CATH LAB ENDO AAA, Medline Kit Number/SKU DYNJ35312J; 6) Product Name CATH LAB ENDO AAA, Medline Kit Number/SKU DYNJ35312K; 7) Product Name OPEN HEART PACK, Medline Kit Number/SKU DYNJ43937; 8) Product Name OPEN HEART PACK, Medline Kit Number/SKU DYNJ80549D; 9) Product Name CV PART 1 AND 2, Medline Kit Number/SKU DYNJ908879; 10) Product Name CV PART 1 AND 2, Medline Kit Number/SKU DYNJ908879C; 11) Product Name CARDIAC SURGERY, Medline Kit Number/SKU DYNJ911589A; 12) Product Name AV SHUNT-MARYVIEW, Medline Kit Number/SKU DYNJ911710; 13) Product Name CARDIAC ACCESSORY PACK, Medline Kit Number/SKU DYNJT7607.

Quantity: 1834 kits

Distribution: US Nationwide distribution.

Recall number Z-0169-2027 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.