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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.

Counts are for the last 30 days.

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Latest recalls

Medicines · Sep 16, 2026 · Class III · Ongoing

Fluphenazine Hydrochloride Tablets, USP, 1mg, 100-count bottles

Ajanta Pharma USA Inc · Bridgewater, NJ, United States

Why: Failed impurities/degradation specifications: (OOS) for Organic Impurities by HPLC (Impurity-A) during testing at the 18 months long term stability. Result: 1.1 percent. Spec: 1.0 percent.

Product details, where it was sold and what to do

Fluphenazine Hydrochloride Tablets, USP, 1mg, 100-count bottles, Rx Only, Marketed by: Ajanta Pharma USA Inc., Bridgewater, NJ 08807, Made in India, NDC 27241-255-01.

Quantity: 403,200 tablets

Distribution: Nationwide within the U.S

Recall number D-0836-2026 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

Epinephrine Injection, USP, 30 mg/30 mL (1mg/mL), 30 mL-Multiple-Dose Vial

American Regent, Inc. · Shirley, NY, United States

Why: Presence of Particulate Matter and Lack of Assurance of Sterility. Particulate matter identified as nylon, cellulosic, acrylic, polyethylene and glass and broken and leaking vials.

Product details, where it was sold and what to do

Epinephrine Injection, USP, 30 mg/30 mL (1mg/mL), 30 mL-Multiple-Dose Vial, Rx Only, For Intravenous Infusion, intramuscular and Subcutaneous Use, AMERICAN REGENT INC., SHIRLEY, NY 11967. NDC 0517-3030-01

Quantity: 31,935 30mL-vials

Distribution: Nationwide within the U.S.A

Recall number D-0865-2026 in the FDA Enforcement Report. Check the lot numbers and dates on your product against the description above.

Medicines · Sep 16, 2026 · Class III · Ongoing

Povidone Iodine 1.25% / Proparacaine HCl 0.5% Ophthalmic Solution, 10 mL per dropper bottle, For Office Use Only, Imprimis NJOF, LLC, 1705 …

ImprimisRx NJ LLC · Ledgewood, NJ, United States

Why: Subpotent Drug

Product details, where it was sold and what to do

Povidone Iodine 1.25% / Proparacaine HCl 0.5% Ophthalmic Solution, 10 mL per dropper bottle, For Office Use Only, Imprimis NJOF, LLC, 1705 Route 46 West, Unit 6B, Ledgewood, NJ 07852, NDC 71384-732-10

Quantity: 772 bottles

Distribution: USA Nationwide

Recall number D-0835-2026 in the FDA Enforcement Report. Check the lot numbers and dates on your product against the description above.

Medicines · Sep 16, 2026 · Class II · Ongoing

FentaNYL Citrate, 1,000 mcg/100 mL (10mcg/mL) Injection solution in 100 mL, 0.9% NaCl Bag, OurPharma LLC, 2512 S

OurPharma LLC · Fayetteville, AR, United States

Why: Labeling: Not Elsewhere Classified: Complaint received on 08/31/2026 regarding the discrepancy of the IV bag expiry (07/31/2026 and 11/30/2026) and the product expiry (12/09/2026).

Product details, where it was sold and what to do

fentaNYL Citrate, 1,000 mcg/100 mL (10mcg/mL) Injection solution in 100 mL, 0.9% NaCl Bag, OurPharma LLC, 2512 S. City Lake, Fayetteville, AR, NDC 73013-1013-01.

Quantity: 1,610 bags

Distribution: Nationwide within the U.S

Recall number D-0864-2026 in the FDA Enforcement Report. Check the lot numbers and dates on your product against the description above.

Food · Sep 16, 2026 · Class II · Ongoing

Fannie May & XO Marshmallow Pixie S'mores Collection, 4.47oz

Ferrero USA · North Canton, OH, United States

Why: Undeclared milk and pecans

Product details, where it was sold and what to do

Fannie May & XO Marshmallow Pixie S'mores Collection, 4.47oz

Quantity: 1488 retail units

Distribution: IA, IL, IN, OH

Recall number H-1334-2026 in the FDA Enforcement Report. Check the lot numbers and dates on your product against the description above.

Food · Sep 16, 2026 · Class I · Ongoing

Alfalfa, Net Weight 50 lbs

International Sprout Holdings, Inc · Cookeville, TN, United States

Why: Potential E. coli and Salmonella contamination

Product details, where it was sold and what to do

Alfalfa, Net Weight 50 lbs. bag, Product of USA, International Specialty Supply 1011 Volunteer Dr. Cookeville, TN 38506

Quantity: 43,799 lbs.

Distribution: Wholesale consignees in 16 states: CA, FL, HI, IL, MA, MN, MO, MT, NY, OH, OR, PA, TN, SC, TX, UT; Puerto Rico; Canada, Mexico, Tahiti, and Venezuela

Recall number H-1341-2026 in the FDA Enforcement Report. Check the lot numbers and dates on your product against the description above.

Food · Sep 16, 2026 · Class I · Ongoing

Momchipz Gluten Free Veggie Chips Broccoli Florets & Cauliflower, net wt

EXOTIQUE FOODS CANADA · Etobicoke, Canada

Why: Undeclared Wheat.

Product details, where it was sold and what to do

Momchipz Gluten Free Veggie Chips Broccoli Florets & Cauliflower, net wt. 3oz (85g). UPC 6 28634 44216 6. Ingredients: Broccoli, Cauliflower, Tapioca Flour, Coconut Oil, Salt, White Pepper. Proudly Made in Indonesia. Imported for Exotique Foods, Inc. Toronto, ON - Canada.

Quantity: 68 cases

Distribution: Product was sold in the U.S.

Recall number H-1330-2026 in the FDA Enforcement Report. Check the lot numbers and dates on your product against the description above.

Food · Sep 16, 2026 · Class II · Ongoing

Prolon Everyday Apulian Almond & Cocoa Spread, NET WT: 8.47 OZ

L-Nutra Inc · Los Angeles, CA, United States

Why: Undeclared allergen (tree nuts): hazelnut, cashew, and pistachio.

Product details, where it was sold and what to do

Prolon Everyday Apulian Almond & Cocoa Spread, NET WT: 8.47 OZ. Product packaged in glass jar with white label and gold screw on closure. UPC: 50040360530

Quantity: 8,529 jars

Distribution: Product is sold exclusively from the recalling firm's online website nationwide.

Recall number H-1335-2026 in the FDA Enforcement Report. Check the lot numbers and dates on your product against the description above.

Food · Sep 16, 2026 · Class I · Ongoing

Crown Farms Dried Suri Cut, 200 gm, in plastic pack, 25 packages per box, keep frozen

EURO FOODS GROUP USA NJ INC · Totowa, NJ, United States

Why: The firm imported and distributed dried ribbon fish that was not properly eviscerated prior to drying.

Product details, where it was sold and what to do

Crown Farms Dried Suri Cut, 200 gm, in plastic pack, 25 packages per box, keep frozen

Quantity: 53 boxes

Distribution: The adulterated product was distributed to the following states: VA, NY, NJ, MI

Recall number H-1331-2026 in the FDA Enforcement Report. Check the lot numbers and dates on your product against the description above.

Consumer products · Sep 10, 2026

ZMC Group Expands Recall of Light-Up Children’s Toys Due to Risk of Serious Injury or Death from Battery Ingestion; Violate Mandatory Standard for Toys

ZMC Group Inc., of Los Angeles, California · China

Why: The recalled light-up toys violate the mandatory safety standard for children’s toys because the toys contain button cell batteries that can be easily accessed by children. 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

Light-Up Children’s Toys. This recall expansion involves ZMC Group battery-operated light-up toys including a Mexican flag theme foam stick, a Unicorn headband, assorted colors and transparent jelly rings and heart shaped balloon flowers. Product Name Item # 19.4" Mexican Flag Theme Light Up Stick SS041-M Light-Up Unicorn Headband G02-UN Light-Up Assorted Colors Jelly Rings PS270 Light-Up Transparent Jelly Rings PS271 Light-Up Heart Balloon Flower 777-1 Packaging for the products has a label with the item number, identification of the distributor, place of manufacture, production date and batch number.

Quantity: About 245,124 (ZMC Group previously recalled 124,560 battery-operated light up toys on May 07, 2026, which are included in the total of 245,124)

Distribution: Sold at Sold At: Diva at Heart, primarily in California, Texas, Oregon, Mississippi, and Arizona, and various distributors and retail stores and online at https://www.divaatheartsj.com/ from October 2018 through July 2026.

Remedy: Consumers should stop using the toys immediately, take them away from children and contact ZMC Group for a full refund. Consumers will be asked to remove the batteries, write “RECALLED” or a large “X” on the product with a permanent marker and submit a photo of the disposed product to recallzmctoy@gmail.com. Note: Button cell batteries are hazardous. Batteries should be disposed of or recycled

Official CPSC recall notice ↗

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Consumer products · Sep 10, 2026

Victgoal Recalls Bicycle Helmets Due to Risk of Serious Injury or Death from Head Injury; Violate Mandatory Standard for Bicycle Helmets

Dongguan Hongtu Sports Goods Co. Ltd., of China · China

Why: The recalled helmets violate the mandatory safety standard for bicycle helmets because the helmets do not comply with the retention system, positional stability and certification requirements. The helmets can fail to protect the user in the event of a crash, posing a serious risk of injury or death due to head injury.

Product details, where it was sold and what to do

Victgoal Children’s Bike Helmets. This recall involves Victgoal-branded bicycle helmets. The red helmets were sold in size small (S), fitting a head circumference of about 19.68 to 21.25 inches. The helmets have red padding, black straps with a silver reflective pattern in the center, a black and red buckle and a black fit-adjusting knob at the back. Only helmets manufactured in November 2025 are included in this recall. "Model HT-006," "Production: 2025/11" and "Ref/Lot# 2025A1101" are printed on a label on the inside of the helmet. "Victgoal" is printed on the product packing bag.

Quantity: About 40

Distribution: Sold at Sold Online At: Walmart.com from March 2026 through June 2026 for between $22 and $36.

Remedy: Consumers should stop using the recalled helmets immediately and contact Victgoal for a full refund. Consumers will be asked to destroy the helmets by cutting the straps and then sending a photo of the destroyed product, showing the helmet’s production date to walmart@victgoal.com. Consumers should then dispose of the recalled product.

Official CPSC recall notice ↗

Consumer products · Sep 10, 2026

Triumph Motorcycles Recalls Closed Course Competition Motorcycles Due to Risk of Serious Injury or Death from Crash Hazard

Triumph Motorcycles America Ltd., of Atlanta, Georgia · Thailand

Why: The engine rocker arm on the recalled motorcycles can seize or stick and the exhaust valves can remain open or break, posing a risk of serious injury or death from a crash hazard.

Product details, where it was sold and what to do

2025 and 2026 Triumph TF450 models Closed Course Competition Motorcycles. This recall involves 2025 and 2026 Triumph TF450 models Closed Course Competition Motorcycles. The motorcycles have a Jet Black/Pure White color scheme. Affected models are TF450-C, TF450-E, TF450-X and TF450RC Edition. The range of affected Vehicle Identification Numbers (VIN) is XXXXXXXXXXXCD4981 to and including XXXXXXXXXXXCP1597. The VIN is located on the vehicle identification plate on the left side of the steering head. Consumers can check if their VIN is included in this recall at https://www.triumphmotorcycles.com/owners/recalls.

Quantity: About 1,560 (In addition, about 171 were sold in Canada)

Distribution: Sold at Sold At: Authorized Triumph Motorcycle Dealers from January 2025 through July 2026 for between $10,000 and $15,000.

Remedy: Consumers should stop using 2025 and 2026 Triumph TF450 models Closed Course Competition Motorcycles immediately and contact Triumph Motorcycles for a free repair. Consumers can check if their VIN is included in this recall at https://www.triumphmotorcycles.com/owners/recalls. Consumers with recalled motorcycles should contact their local authorized Triumph Motorcycle dealer who will inspect the e

Official CPSC recall notice ↗

Consumer products · Sep 10, 2026

Sweet Cubby Recalls Children's Loungewear Sets Due to Risk of Serious Injury or Death from Burn Hazard; Violate Mandatory Standard for Children's Sleepwear

Hong Kong Xuheyuan Trading Co., Ltd, dba Sweet Cubby, of China · China

Why: The recalled children’s loungewear sets violate the mandatory flammability standard for children’s sleepwear, posing a risk of serious burn injuries or death.

Product details, where it was sold and what to do

Sweet Cubby Children’s Loungewear Sets. This recall involves all Sweet Cubby children's loungewear sets. The recalled two-piece loungewear sets consist of a short-sleeved shirt and matching shorts. The sets were sold in various colors and in children's sizes 5-6Y through 13-14Y. "Batch No.: 272779" and the size are printed on the sewn-in neck label and on the seam label.

Quantity: About 12,461

Distribution: Sold at Sold Online At: SHEIN.com from June 2025 through May 2026 for between $8 and $12.

Remedy: Consumers should stop using the recalled loungewear sets immediately, take them away from children and contact Sweet Cubby for a full refund. Consumers will be asked to destroy the loungewear sets by cutting them in half and send a photo of the destroyed loungewear sets to SweetCubby@163.com. Consumers should then dispose of the destroyed product.

Official CPSC recall notice ↗

Consumer products · Sep 10, 2026

SQT Recalls Lontcs Busy Boards Due to Risk of Serious Injury from Lead Poisoning; Violate Federal Lead Paint Ban

Xianyouxianlichengshaungqiaotouqichemeirongdian (Xianyou County Licheng Shuangqiaotou Auto Beauty Shop), dba SQT LLC, of China · China

Why: The toys’ zipper contains levels of lead that exceed the standard set in the federal lead paint ban. Lead is toxic if ingested by young children and can cause adverse health issues.

Product details, where it was sold and what to do

Lontcs Busy Board. This recall involves the Lontcs Busy Board toys. The toys consist of a wood board and metal handle with multiple attached components including a black plastic buckle with cream colored straps; a brown zipper; a metal latch; a caster wheel; a white doorbell; a lock with keys; a music box with crank; a zig zag duck puzzle; an abacus with three rows of white; red and tan beads; and a white fidget spinner.

Quantity: About 1,835

Distribution: Sold at Sold Online At: Amazon.com from May 2024 through July 2026 for about $31.

Remedy: Consumers should stop using the busy boards immediately and contact SQT for a full refund. Consumers will be asked to destroy the toys by unscrewing its components, write in permanent marker “RECALLED” on the board, and send a photo of the destroyed toy to Lontcs@163.com. Consumers should then dispose of the destroyed product.

Official CPSC recall notice ↗

Consumer products · Sep 10, 2026

Ricky Joy Recalls More Than 2.3 Million Sour Crush Candy Bottles Due to Risk of Serious Injury or Death from Choking Hazard

International Trade Imports LLC (The Ricky Joy Company), dba Ricky Joy, of Cumming, Georgia · Colombia

Why: The rolling ball on the recalled candy bottles can detach, posing a risk of serious injury or death from choking hazard.

Product details, where it was sold and what to do

Ricky Joy Sour Crush Rolling Liquid Candy Bottles. This recall involves Ricky Joy-branded Sour Crush Rolling Liquid Candy bottles. The bottles contain 1.85 fluid ounce of sour liquid candy intended to be applied through the bottle's rollerball top. The plastic candy bottles were sold individually and in packs of three or 12 bottles per pack, and in the following colors/flavors: blue (blue raspberry), red (strawberry), green (green apple) and pink (watermelon). The Ricky Joy logo, "EXTREME SOUR", "SOUR CRUSH" and the flavor name are printed on the front of the bottle, along with the image of a green monster.

Quantity: About 2.3 million

Distribution: Sold at Sold At: H-E-B, Forman Mill and other candy stores nationwide and online at Walmart.com, CandyFunHouse.com, RickyJoy.com and other online retailers from January 2023 through May 2026 for about $3 for the bottle and for between $13 and $32 for the pack.

Remedy: Consumers should stop using the candy bottles immediately, take them away from children and contact The Ricky Joy Company for a refund. Consumers will be provided with a pre-paid shipping label to return the recalled product.

Official CPSC recall notice ↗

Consumer products · Sep 10, 2026

Prepared Hero Recalls Fire Spray Canisters Due to Risk of Serious Injury or Death from Fire and Burn Hazards

Prepared Hero, of Sheridan, Wyoming · China

Why: The recalled fire spray canister can deteriorate overtime, causing it to rupture and fail to operate during a fire, posing the risk of serious injury or death from fire and burn hazards.

Product details, where it was sold and what to do

Hero Fire Spray Canisters. This recall involves the Hero Fire Spray Fire Canisters. The canisters are either red and blue or red and have the company's logo on them with the name HERO Fire Spray on the front panel of the spray. Each canister contains 20 fluid ounces. The circular canisters are about 2.6 inches in diameter and 11.4 inches tall and weigh about 1.8 pounds. There is a black plastic release tab on the top of the canister. The affected batch is clearly marked on the base of the canister with the numbers "09/2024" as the date code.

Quantity: About 31,000

Distribution: Sold at Sold Online At: PreparedHero.com and Amazon.com from October 2024 through January 2026 for between $18 to $30.

Remedy: Consumers should stop using the fire spray canisters immediately and visit www.preparedhero.com/pages/recall for instructions on how to receive a free replacement unit and how to properly dispose of the recalled fire spray canister according to local and state regulations. Consumers will be asked to place their fire spray canister in a box, label the box “RECALLED”, and bring it to a municipal ho

Official CPSC recall notice ↗

Consumer products · Sep 10, 2026

Junkins Recalls DHASUWT Hair Dryer Brushes Due to Risk of Serious Injury or Death from Electrocution, and Shock Hazards; Violate Federal Regulations; Smoking and Fire Hazards

Shenzhen Weihua Chenyu Technology Co., Ltd, dba Junkins, of China · China

Why: The recalled hair dryer brushes lack an integrated immersion protection device, which presents a substantial product hazard to consumers, posing the risk of death or serious injury from electrocution or shock if the hair dryers fall into water while plugged in to an electrical source. The recalled hair dryer brushes also pose the risk of death or serious injury from smoking and fire hazards.

Product details, where it was sold and what to do

DHASUWT Hair Dryer and Blow Dryer Brushes. This recall involves DHASUWT Hair Dryer and Blow Dryer Brush in 1, Negative Ion Hair Dryer Brush, 1Step Ionic Hair Straightener Brush Hair Dryer Hot Air Brush, Hair Styling Tool Straightening Dryer, with model number XR-8801. The hair dryers are black hot air dryer paddle brushes with a pink design and brush bristles. There are three heat settings on the hair dryers. The top of the product packaging is labeled XRUI with the model name XR-8801.

Quantity: About 1,738

Distribution: Sold at Sold At: Amazon.com from October 2024 through June 2026 for about $27

Remedy: Consumers should unplug and stop using the recalled hair dryers immediately and contact Junkins to receive a full refund. Consumers will be asked to cut the power cord and provide a photo of the destroyed product to DHASUWT_recall@163.com.

Official CPSC recall notice ↗

Consumer products · Sep 10, 2026

Guang Zhou Recalls Wantefully Hair Dryer Brushes Due to Risk of Serious Injury or Death from Electrocution, Shock and Burn Hazards; Violate Federal Regulations

Guang Zhou Shi Wan Te Fu Ke Ji You Xian Gong Si, dba Wantefully, of China · China

Why: The recalled hair dryer brushes are in violation of federal regulations for hair dryers as they lack an integrated immersion protection device, which presents a substantial product hazard to consumers and the risk of death or serious injury from electrocution or shock if the hair dryers fall into water while plugged in. In addition, the recalled hair dryer brushes can overheat, posing a burn hazard.

Product details, where it was sold and what to do

Wantefully Hair Dryer Brushes. This recall involves Wantefully 2 in 1 Hair Dryer & Styler, One Step Hair Dryer Brush Straightner, and the Negative Ion Electric Hot Air Blow Dryer Comb, model number XR-8801. The hair dryers are black hot air dryer paddle brushes with a striped pink design and brush bristles. There are three heat settings on the hair dryers. XRUI and the model name XR-8801 are printed on the top of the product packaging.

Quantity: About 2,295

Distribution: Sold at Sold Online At: Amazon.com from February 2026 through March 2026 for about $30.

Remedy: Consumers should unplug and stop using the recalled hair dryers immediately and contact Guang Zhou to receive a full refund. Consumers will be asked to cut the power cord and provide a photo of the destroyed product to wantefully@163.com.

Official CPSC recall notice ↗

Consumer products · Sep 10, 2026

FJTJBSI Recalls Six-Drawer Dressers Due to Risk of Serious Injury or Death from Tip-Over and Entrapment Hazards; Violate Mandatory Standard for Clothing Storage Units

Fujian Laobosi Cross-Border E-commerce Co., Ltd., dba FJTJBSI, of China · China

Why: The recalled dressers are unstable if they are not anchored to the wall, posing tip-over and entrapment hazards that can result in risks of serious injuries or death to children. The dressers violate the mandatory safety standards as required by the STURDY Act.

Product details, where it was sold and what to do

FJTJBSI Six-drawer Dressers. This recall involves the FJTJBSI-branded wood dressers. The black or white dressers measure about 15.1 inches long, 27.6 inches wide and 42.2 inches high, and weigh 68 pounds. The dressers have six drawers with silver or black handles. "LBS-XD-4-2-BLK-023" or "LBS-XD-4-2-WIT-024" is printed on a label on the product packaging.

Quantity: About 9,000

Distribution: Sold at Sold Online At: Amazon.com from November 2024 through July 2026 for about $170.

Remedy: Consumers should stop using the recalled dressers immediately if they are not anchored to the wall, place them in an area that children cannot access and contact FJTJBSI for a full refund. Consumers will be asked to write in permanent marker “RECALLED” on the dresser and send a photo of the marked dresser to FJTJBSIrecall@outlook.com. Consumers should then dispose of the recalled product.

Official CPSC recall notice ↗

Consumer products · Sep 10, 2026

Dual Fuel Ranges Recalled Due to Risk of Serious Injury or Death from Fire or Explosion Hazards; Manufactured by AGA Rangemaster

AGA Rangemaster Limited, of United Kingdom · United Kingdom

Why: Dual Fuel Ranges with a missing cap from the gas test port can cause a gas leak,​ posing a risk of serious injury or death from fire or explosion hazards.

Product details, where it was sold and what to do

AGA Elise and Mercury Series Freestanding Dual Fuel Ranges and La Cornue CornuFé 90 and CornuFé 110 Series Freestanding Dual Fuel Ranges. This recall involves freestanding AGA Elise and Mercury Series Dual Fuel Ranges, in 36- and 48-inch widths and freestanding La Cornue CornuFé Series Dual Fuel Ranges in 36- and 43-inch widths manufactured between March 19, 2025 and July 24, 2026. All units have gas surface burners, set for Natural or LP gas, with one to three electric ovens depending on size.  The products are sold in stainless steel, white and 13 other colors, which can be found at www.agarangeusa.com and www.lacornueusa.com. All colors, trim options and gas types (Natural or LP) are included.  The serial number is on the rating plate, which is located on the bottom panel of the unit under the storage drawer.

Quantity: About 3,992 (In addition, about 336 were sold in Canada)

Distribution: Sold at Sold At: Authorized appliance dealers nationwide from March 2025 through July 2026 for about $6,000 to $20,000.

Remedy: Consumers should shut off the gas supply to avoid the risk of gas leak immediately and contact AGA Rangemaster. Consumers should promptly determine if their range is subject to recall by locating the model/serial number on the rating plate (on the bottom panel under the storage drawer) and visiting the Recall webpage at www.lacornueusa.com/testcap-recall or www.agarangeusa.com/testcap-recall. If

Official CPSC recall notice ↗

Consumer products · Sep 10, 2026

Cade California Electronic Recalls Finger Light Toys Due to Risk of Serious Injury or Death from Battery Ingestion; Violate Mandatory Standard for Toys

California Cade Electronic, LLC, of Hacienda Heights, California · China

Why: The recalled finger lights violate the mandatory safety standard for toys because the toys contain button cell batteries that can be easily accessed by children. 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

Cade California Electronic Projecting Finger Light Toys. This recall involves California Cade Electronic Finger Lights, which contain three button cells batteries. The finger lights come in 50 pieces in a box in white, blue, red and green. The finger lights have "California Cade Electronic" and "Finger Flashlights" printed on labels located on the front of the package.

Quantity: About 179,739

Distribution: Sold at Sold At: Amazon.com from March 2015 through July 2026 for between $5 and $16.

Remedy: Consumers should stop using the recalled toys immediately, take them away from children and contact Cade California Electronic for a full refund. Consumers will be asked to properly dispose of the finger lights into the trash and send a photo of the disposed product to ccecamazonservice@gmail.com. Note: Button cell batteries are hazardous. Batteries should be disposed of or recycled by followin

Official CPSC recall notice ↗

Medical devices · Sep 9, 2026 · Class II · Ongoing

Medline Convenience Kits: 1) BLOOD DRAW KIT, Catalog Number: DYLAB1081; 2) WHOLE BLOOD PHLEBOTOMY KIT, Catalog Number: DYNDB3005D

Medline Industries, LP · Northfield, IL, United States

Why: The kits contain BD ChloraPrep Clear - 1 mL and FREPP Clear 1.5 mL Applicators which have a potential breach of sterility in the packaging, due to wrinkles in the paper lidding which may extend to the seal area. If the sterile barrier is compromised, patients and users may be exposed to microbial contamination. Potential health consequences may include no injury, localized infection, or, less commonly, more serious …

Product details, where it was sold and what to do

Medline Convenience Kits: 1) BLOOD DRAW KIT, Catalog Number: DYLAB1081; 2) WHOLE BLOOD PHLEBOTOMY KIT, Catalog Number: DYNDB3005D; 3) QP KIT, Catalog Number: DYNDB3005F; 4) DOUBLE RED CELL PHLEBOTOMY KIT, Catalog Number: DYNDB3006C; 5) PLATELET PHLEBOTOMY KIT, Catalog Number: DYNDB3007C; 6) WHOLE BLOOD KIT, Catalog Number: DYNDB3041D; 7) PHLEBOTOMY, Catalog Number: DYNDB3044D; 8) PHLEBOTOMY, Catalog Number: DYNDB3044F; 9) DONATION - WB, Catalog Number: DYNDB3086D; 10) DONATION - ALYX/TRIMA W/O TOUR, Catalog Number: DYNDB3088B; 11) THERAPEUTIC NFT, Catalog Number: DYNDB3100; 12) BLOOD CULTURE TRAY ADULT, Catalog Number: DYNDH1194A; 13) ADULT BLOOD CULTURE KIT, Catalog Number: DYNDH1444D; 14) PEDS BLOOD CULTURE KIT, Catalog Number: DYNDH1445C; 15) BLOOD CULTURE KIT, Catalog Number: DYNDH1462B; 16) BLOOD CULTURE ADULT, Catalog Number: DYNDH1619A; 17) BLOOD CULTURE PEDI, Catalog Number: DYNDH1620A; 18) BLOOD CULTURE KIT, Catalog Number: DYNDH1622C; 19) BLOOD CULTURE KIT, Catalog Number: DYNDH1622D; 20) BLOOD CULTURE COLLECTION KIT, Catalog Number: DYNDH1626B; 21) ADULT BLOOD CULTURE KIT, Catalog Number: DYNDH1694A; 22) ADULT BLOOD CULTURE KIT, Catalog Number: DYNDH1695; 23) BLOOD CULTURE KIT, Catalog Number: DYNDH1708A; 24) BLOOD CULTURE COLLECTION KIT, Catalog Number: DYNDH1714A; 25) BLOOD CULTURE KIT, Catalog Number: DYNDH1715B; 26) BLOOD CULTURE KIT, Catalog Number: DYNDH1723; 27) NS BLOOD CULTURE 23G KIT, Catalog Number: D…

Quantity: 996692 kits

Distribution: US Nationwide distribution.

Recall number Z-3063-2026 in the FDA Enforcement Report. Check the lot numbers and dates on your product against the description above.

Medical devices · Sep 9, 2026 · Class II · Ongoing

Presource Packs Containing CliniClean Pericare Wipes within BD Urinary Catheter Trays: 1) KIT, GVI OPEN HEART A B , Catalog Number: PCVNCG5…

Cardinal Health 200, LLC · Waukegan, IL, United States

Why: The Urinary Catheter Trays contain CliniClean Pericare Wipes which may potentially be contaminated with a lubricant used during the manufacturing process. If a contaminated wipe is used on a patient, localized skin effects may occur. These may include irritation, erythema, or mild inflammation.

Product details, where it was sold and what to do

Presource Packs Containing CliniClean Pericare Wipes within BD Urinary Catheter Trays: 1) KIT, GVI OPEN HEART A B , Catalog Number: PCVNCG540; 2) KIT, GVI OPEN HEART A B , Catalog Number: PCVNCG542; 3) KIT, GVI OPEN HEART A B , Catalog Number: PCVNCG55I; 4) KIT, BLO BASIC OPEN HEART , Catalog Number: PVCGBOB10; 5) KIT, BLO BASIC OPEN HEART , Catalog Number: PVCGBOB10; 6) KIT, BLO BASIC OPEN HEART , Catalog Number: PVCGBOB12; 7) KIT, BLO BASIC OPEN HEART , Catalog Number: PVCGBOB17; 8) KIT, OPEN HEART CON , Catalog Number: PVCGOHCOH; 9) KIT,OPEN HEART ADULT MDST , Catalog Number: PVCGOHCPA; 10) KIT, CABG , Catalog Number: PVHDCBAGK; 11) KIT, ORP CABG , Catalog Number: PVHDCGVCP; 12) KIT, ORP CABG , Catalog Number: PVHDCGV40; 13) KIT, VALVE , Catalog Number: PVHDVAAGH; 14) KIT, ORP VALVE , Catalog Number: PVHDVPVCQ; 15) KIT, ORP VALVE , Catalog Number: PVHDVPV43; 16) KIT, MAJOR CARDIAC , Catalog Number: PVOCMGJ36; 17) KIT, OPEN HEART DH , Catalog Number: PVOCOHNHE; 18) KIT, OPEN HEART , Catalog Number: PVOCOH12O; 19) KIT, CAROTID ENDARTERECTOMY , Catalog Number: PVVMCV07E; 20) KIT, FEM POP BARNES JEW , Catalog Number: PVVMFP22R; 21) KIT, FEM POP BARNES JEW , Catalog Number: PVVMFP245; 22) KIT, THORACIC BARNES JEWISH , Catalog Number: PVV…

Quantity: 2448 units

Distribution: US Nationwide distribution.

Recall number Z-3098-2026 in the FDA Enforcement Report. Check the lot numbers and dates on your product against the description above.

Medical devices · Sep 9, 2026 · Class II · Ongoing

Medline Convenience Kits containing BD ChloraPrep Clear - 1mL Applicators PAIN PRE OP KIT DYKS1476A

Medline Industries, LP · Northfield, IL, United States

Why: Convenience kits contain BD ChloraPrep Clear - 1mL Applicators from specific lots that were recalled by the manufacturer because they may have an open or incomplete seal on the applicator packaging. Use of potentially contaminated applicator may lead to localized skin or soft tissue infection, or systemic infection or infectious complications.

Product details, where it was sold and what to do

Medline Convenience Kits containing BD ChloraPrep Clear - 1mL Applicators PAIN PRE OP KIT DYKS1476A

Quantity: 222,653 total

Distribution: US Nationwide distribution.

Recall number Z-3067-2026 in the FDA Enforcement Report. Check the lot numbers and dates on your product against the description above.

Medical devices · Sep 9, 2026 · Class II · Ongoing

Medline Convenience Kits: 1) ORTHO ASPIRATION KIT, Model Number: DYKM1636A

Medline Industries, LP · Northfield, IL, United States

Why: The kits contain BD ChloraPrep Clear - 1 mL and FREPP Clear 1.5 mL Applicators which have a potential breach of sterility in the packaging, due to wrinkles in the paper lidding which may extend to the seal area. If the sterile barrier is compromised, patients and users may be exposed to microbial contamination. Potential health consequences may include no injury, localized infection, or, less commonly, more serious …

Product details, where it was sold and what to do

Medline Convenience Kits: 1) ORTHO ASPIRATION KIT, Model Number: DYKM1636A; 2) SHOULD BLOCK KIT, Model Number: DYKM1881A; 3) TRIMA KIT, Model Number: DYNDB3077C

Quantity: 18290 kits

Distribution: US Nationwide distribution.

Recall number Z-3062-2026 in the FDA Enforcement Report. Check the lot numbers and dates on your product against the description above.

Medical devices · Sep 9, 2026 · Class II · Ongoing

1) NEURO, (kit) ACNE73-01; 2) NEURO, (kit) ACNE73-03; 3) CRANI, (kit) AKCR19-01; 4) ORTHO SPINE PACK, (kit) ARMC017; 5) BMHM NEURO PACK, (k…

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

Why: The recall notice was initiated due to a Medicom Urgent Medical Device Recall. Medicom is recalling specific lots of Ritmed¿ Neurological Sponges Non-Sterile Models 55992C to 55998C due to potential for unexpected variability of endotoxin levels on the products.

Product details, where it was sold and what to do

1) NEURO, (kit) ACNE73-01; 2) NEURO, (kit) ACNE73-03; 3) CRANI, (kit) AKCR19-01; 4) ORTHO SPINE PACK, (kit) ARMC017; 5) BMHM NEURO PACK, (kit) BMHT016-05; 6) LUMBAR PACK, (kit) BMHT112-03; 7) NEURO LAMINECTOMY PACK, (kit) DGNE75; 8) NEURO LAMINECTOMY PACK, (kit) DGNE75-02; 9) DRAH NEURO LAMINECTOMY SNEDHDN,(kit) DRNE75; 10) DRAH NEURO LAMINECTOMY SNEDHDN, (kit) DRNE75-01; 11) CRANIOSYNOSTOSIS CUSTOM SNE23C, (kit) DUCR36-01; 12) CRANIOSYNOSTOSIS CUSTOM SNE23C, (kit) DUCR36-02; 13) NEURO CRANIOTOMY PK SNE23C1116, (kit) DUNC42-01; 14) PEDS NEURO PACK SNE2301147, (kit) DUNE88-01; 15) NEURO SPINE PACK SNE23LM110, (kit) DUSP98-01; 16) NEURO SPINE PACK SNE23LM110, (kit) DUSP98-02; 17) CRANI PACK 712638, (kit) EFCR86-01; 18) SPINE PACK 712040, (kit) EFSP30-01; 19) SPINE PACK 712040, (kit) EFSP30-02; 20) CRANIOTOMY TRAY, (kit) EURO009-09; 21) CRANI PACK, (kit) IHCR36-01; 22) NEURO PACK, (kit) IHNE35-01; 23) CRANIOTOMY PACK, (kit) JACK410-11; 24) BASIC NEURO PACK, (kit) MAMC275-06; 25) BASIC NEURO PACK, (kit) MAMC275-07; 26) SPINE CRANI PACK, (kit) MCSP92-01; 27) CRANIOTOMY PACK, (kit) MECP05R; 28) SPINE TRAY GLOBALMICROSURG, (kit) MEDF217-02; 29) NEURO BASIC PACK, (kit) MENE06T; 30) CRANIAL PACK - 205992, (kit) MHCP75-01; 31) NEURO PACK, (kit) MMOK007-03; 32) NEURO PACK, (kit) MMTN012-04; 33) CRANIOTOMY PACK SNECGCRM11, (kit) MSMC108-01; 34) NEURO ANT CERV LAMI ADD A PACK, (kit) NAMC413-07; 35) STRL NEURO LUMB LAMI…

Quantity: 16223 kits

Distribution: US Nationwide distribution in the states of AZ, CA, CO, WA, WY, TX, MI, FL, MD, UT, NC, MS, PA, MO, IA, NE, OH, IL, SD, MN, GA.

Recall number Z-3045-2026 in the FDA Enforcement Report. Check the lot numbers and dates on your product against the description above.

Medical devices · Sep 9, 2026 · Class II · Ongoing

Presource Packs Containing CliniClean Pericare Wipes within BD Urinary Catheter Trays: 1) KIT,GYN LAPAROSCOPY DH , Catalog Number: PBOCGLN17

Cardinal Health 200, LLC · Waukegan, IL, United States

Why: The Urinary Catheter Trays contain CliniClean Pericare Wipes which may potentially be contaminated with a lubricant used during the manufacturing process. If a contaminated wipe is used on a patient, localized skin effects may occur. These may include irritation, erythema, or mild inflammation.

Product details, where it was sold and what to do

Presource Packs Containing CliniClean Pericare Wipes within BD Urinary Catheter Trays: 1) KIT,GYN LAPAROSCOPY DH , Catalog Number: PBOCGLN17

Quantity: 36 units

Distribution: US Nationwide distribution.

Recall number Z-3094-2026 in the FDA Enforcement Report. Check the lot numbers and dates on your product against the description above.

Medical devices · Sep 9, 2026 · Class II · Ongoing

Presource Packs Containing CliniClean Pericare Wipes within BD Urinary Catheter Trays: 1) KIT, LUNG TX CIRCULATOR , Catalog Number: OVC3507…

Cardinal Health 200, LLC · Waukegan, IL, United States

Why: The Urinary Catheter Trays contain CliniClean Pericare Wipes which may potentially be contaminated with a lubricant used during the manufacturing process. If a contaminated wipe is used on a patient, localized skin effects may occur. These may include irritation, erythema, or mild inflammation.

Product details, where it was sold and what to do

Presource Packs Containing CliniClean Pericare Wipes within BD Urinary Catheter Trays: 1) KIT, LUNG TX CIRCULATOR , Catalog Number: OVC3507231

Quantity: 19 units

Distribution: US Nationwide distribution.

Recall number Z-3096-2026 in the FDA Enforcement Report. Check the lot numbers and dates on your product against the description above.

Medical devices · Sep 9, 2026 · Class II · Ongoing

LUX-Dx, LUX-Dx II, LUX-Dx II+ Insertable Cardiac Monitor System, SERVER SW LAT CLARITY DS EU, Model Number 7246, All Versions (Current 7.7)

Boston Scientific Corporation · Saint Paul, MN, United States

Why: There is potential for a delay in AF Burden Alert notification affecting the server software which supports the Insertable Cardiac Monitors (ICMs). Delayed notification of an AF Burden Alert may delay clinical evaluation or therapeutic intervention of an atrial arrhythmia.

Product details, where it was sold and what to do

LUX-Dx, LUX-Dx II, LUX-Dx II+ Insertable Cardiac Monitor System, SERVER SW LAT CLARITY DS EU, Model Number 7246, All Versions (Current 7.7)

Quantity: N/A

Distribution: Worldwide - US Nationwide distribution.

Recall number Z-3082-2026 in the FDA Enforcement Report. Check the lot numbers and dates on your product against the description above.

Medical devices · Sep 9, 2026 · Class II · Ongoing

Medline Convenience Kits containing BD ChloraPrep Clear - 1mL Applicators LABOR CDS CDS981762B VAG DELIVERY ADMISSION BAG DYKA1054F

Medline Industries, LP · Northfield, IL, United States

Why: Convenience kits contain BD ChloraPrep Clear - 1mL Applicators from specific lots that were recalled by the manufacturer because they may have an open or incomplete seal on the applicator packaging. Use of potentially contaminated applicator may lead to localized skin or soft tissue infection, or systemic infection or infectious complications.

Product details, where it was sold and what to do

Medline Convenience Kits containing BD ChloraPrep Clear - 1mL Applicators LABOR CDS CDS981762B VAG DELIVERY ADMISSION BAG DYKA1054F

Quantity: 222,653 total

Distribution: US Nationwide distribution.

Recall number Z-3076-2026 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.