These recalls involve products that pose serious risks of injury or death. Check if you own any of these products and take immediate action if needed.

High Risk Recalls

3,609 critical product recalls that require immediate attention. These products have been identified as posing serious safety hazards.

What to do if you own a recalled product:

  1. Stop using the product immediately
  2. Keep the product away from children
  3. Follow the remedy instructions provided
  4. Contact the manufacturer for a refund or replacement
Health & Personal Care
HIGH
FDA DEVICE

Olympus MAJ-210 Single-Use Biopsy Valve Recalled for 95,882 Boxes Nationwide (2026)

Olympus Corporation of the Americas recalls 95,882 boxes of MAJ-210 single-use biopsy valves distributed nationwide to hospitals and clinics in the United States after reports of rubber fragments detaching during use. The defect can release fragments into the endoscope channel or patient. Healthcare facilities should stop using the device immediately and follow recall instructions.

Olympus
Potential for
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Recalled Teether Toy – Red
HIGH
CPSC

AiTuiTui Pull String Teething Toys Recalled for Choking Hazard

AiTuiTui recalled its Pull String Teething Toys on January 29, 2026, due to a choking risk. The toys do not meet mandatory safety standards, posing a potential risk of serious injury or death. Consumers should stop using the teething toys immediately and contact the manufacturer for a refund.

AiTuiTui Pull String Teething Toys
The hair
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Food & Beverages
HIGH
FDA FOOD

Preema Food Colour Powder Recalled Over Banned Ingredients

Preema brand recalled 720 bottles of Bright Red and Orange Food Colour Powders on January 29, 2026. The products contain a banned color, carmoisine, and undeclared FD&C Yellow 5 and FD&C Red 40. Consumers should not consume these products and seek refunds immediately.

KPCM New York
Products contain
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NorthStar Gas Wet Steam and Hot Water Pressure Washer (Item #157310)
HIGH
CPSC

Northern Tool Recalls Hot Water Pressure Washers Over Fire Risk

Northern Tool + Equipment recalled three models of hot water pressure washers on January 29, 2026. Abnormal burner operation can produce smoke and flames, posing a fire hazard. Consumers should stop using the products immediately and seek repairs.

Northern Tool + Equipment Manufacturing, of Faribault, Minnesota
The fan
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Recalled Sefudun 5% Minoxidil Hair Growth Serum Kit for Men
HIGH
CPSC

Sefudun Hair Growth Serum Recalled Due to Child Poisoning Risk

Nengmiaokeji recalled Sefudun 5% Minoxidil Hair Growth Serum Kit on January 29, 2026. The product lacks child-resistant packaging, posing a serious poisoning risk to children. Consumers should stop using the serum immediately and contact the company for a replacement.

Sefudun
The hair
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Recalled Mindbodygreen Ultimate Multivitamin+ Dietary Supplement Bottle
HIGH
CPSC

Mindbodygreen Recalls Multivitamin Due to Child Poisoning Risk

Mindbodygreen recalled Ultimate Multivitamin+ dietary supplements on January 29, 2026, due to a risk of child poisoning. The bottles lack child-resistant packaging, violating safety standards. Consumers should stop using the product immediately and secure it out of children's reach.

Arizona Nutritional Supplements, of Chandler, Arizona
The bottles
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Violative LuxJet Submersible LED Lights
HIGH
CPSC

LuxJet LED Lights Recalled Due to Battery Ingestion Risk

LuxJet recalled Submersible LED Lights on January 29, 2026, due to ingestion risks from lithium batteries. The recall affects sets of 10 lights sold with multiple batteries. Consumers must stop using the lights and return them for a refund.

LuxJet Submersible LED Lights
The recalled
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Health & Personal Care
HIGH
FDA DRUG

Teva Metoprolol Succinate 50 mg Extended-Release Recall 2026 Following Failed Dissolution Specs (67,

Teva Pharmaceuticals recalled 67,043 bottles of Metoprolol Succinate Extended-Release Tablets, 50 mg, distributed nationwide. The FDA enforcement report cites Failed Dissolution Specifications as the hazard. Health care providers and patients should stop using this product immediately and contact Teva for guidance.

METOPROLOL SUCCINATE
Failed Dissolution
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Recalled Bazic Silicone Glue – Front and Side
HIGH
CPSC

Bazic Products Recalls Silicone Glue Over Child Poisoning Risk

Bazic Products recalled Bazic Silicone Glue on January 29, 2026, due to a serious poisoning risk for children. The glue's packaging does not meet child-resistant standards, violating federal law. Consumers should stop using the product immediately and seek a full refund.

Bazic Products
The glue
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Health & Personal Care
HIGH
FDA DRUG

Teva Metoprolol Succinate ER 100 mg Recall Expanded for Failed Dissolution Specifications (2026)

Teva Pharmaceuticals recalled 7,448 bottles of Metoprolol Succinate Extended-Release Tablets nationwide after failed dissolution specifications were identified. The recall involves 100 mg, 100‑tablet bottles (NDC 45963-677-11) and 1,000‑tablet bottles (NDC 45963-677-96). The defect may affect drug release and efficacy. Patients should stop using affected bottles and contact Teva or their clinician

METOPROLOL SUCCINATE
Failed Dissolution
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Food & Beverages
HIGH
FDA FOOD

Koi Koi Trading Recalls Fish Balls Over Allergen Risk

Koi Koi Trading recalled 8,232 cases of frozen fish balls on January 28, 2026. The product contains undeclared wheat and sesame allergens, posing a serious health risk. Consumers should check their freezers and take immediate action.

MIN JIANG FOOD STORE INC DBA KOI KOI TRADING
Undeclared allergen
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Food & Beverages
HIGH
FDA FOOD

Koi Koi Trading Recalls Fish Balls Due to Undeclared Allergens

Koi Koi Trading recalled 3,884 cases of frozen fish balls on January 28, 2026. The recall was issued due to undeclared allergens, Wheat and Sesame, posing a serious health risk. Consumers should stop using the product immediately and seek a refund.

MIN JIANG FOOD STORE INC DBA KOI KOI TRADING
Undeclared allergen
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Food & Beverages
HIGH
FDA FOOD

Why Not Natural Recalls Moringa Capsules Due to Salmonella Risk

Art Monkey LLC recalled 8,500 bottles of Why Not Natural Moringa Capsules on January 28, 2026. The capsules may be contaminated with Salmonella and pose a serious health risk. Consumers should stop using the product immediately and seek refunds.

Art Monkey LLC dba Why Not Natural
Potential to
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Food & Beverages
HIGH
FDA FOOD

Koi Koi Trading Recalls Fish Balls Due to Allergen Risk

Koi Koi Trading recalled 344 cases of frozen fish balls on January 28, 2026. The product contains undeclared allergens, wheat and sesame, posing a serious risk to consumers. The recall affects distribution in eight states including California and Texas.

MIN JIANG FOOD STORE INC DBA KOI KOI TRADING
Undeclared allergen
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Health & Personal Care
HIGH
FDA DEVICE

23,568 Medline Surgical Drapes Recalled Over Infection Risk

Medline Industries recalled 23,568 surgical drapes on January 28, 2026, after reports of fabric delamination during laundering. The delamination may delay patient care and increase the risk of infection. Health care providers and facilities must stop using these drapes immediately and follow the manufacturer's instructions for a remedy.

Medline Industries, LP
Fabric may
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Health & Personal Care
HIGH
FDA DEVICE

Medline Medcrest Surgical Gowns Recalled 104,004 Units for Delamination Risk (2026)

Medline recall covers 104,004 Medcrest Surgical Gowns sold nationwide and internationally due to premature fabric delamination risk. Delamination can delay patient care in surgery and raise infection risk. Stop using the affected gowns and follow the manufacturer’s recall instructions immediately.

Medline Industries
Fabric may
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