chemical hazard Recalls

1,078 recalls tagged with “chemical hazard”.

Health & Personal Care
HIGH
FDA DEVICE

Medline Chest Drainage Units Recall Updated IFUs for Adults 18+

Medline Industries recalls 2,894 Aqua-Seal Chest Drainage Units from Cardinal Health after updating IFUs to specify adult patients 18 years and older. The devices were distributed worldwide, including California, Chile and Panama. The update clarifies intended patient population and requires action from healthcare providers to stop use until further notice.

Medline Industries, LP
The instructions
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Food & Beverages
HIGH
FDA FOOD

Reser's Tuna Salad Recalled Over Undeclared Fish Allergen

Reser's Fine Foods recalled 298 tubs of Tuna Salad on January 30, 2026 due to undeclared fish allergens. The product was mislabeled with a Chicken Salad lid, posing a risk to consumers with fish allergies. The recall affects distribution in Arizona, California, Nevada, Utah, and Washington.

Reser's Fine Foods
Undeclared fish
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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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Recalled VIOFAIRY Hair Growth Serum bottle and packaging
HIGH
CPSC

Viofairy Hair Growth Serum Recalled Over Child Poisoning Risk

Viofairy recalled its Hair Growth Serum on January 29, 2026, due to serious poisoning risks. The packaging lacks required child-resistant features, endangering young children. Consumers must stop using the product immediately and secure it out of reach.

Guangzhou Runshu BioTech Co., Ltd. of China
The serum
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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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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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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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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 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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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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Health & Personal Care
HIGH
FDA DEVICE

BD 10 mL Luer-Lok Syringe Recalled Over Bundle Packaging Mix-Up in US; 204,000 Units Affected

BD recalled 204,000 10 mL Luer-Lok/Luer Slip syringes due to a packaging mix-up that placed Luer Slip syringes in a batch designated for Luer Lok syringes. The nationwide recall covers products distributed in California and Texas. Healthcare providers and patients should stop using the affected syringes immediately and consult manufacturer recall instructions.

Becton Dickinson
During the
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Food & Beverages
HIGH
FDA FOOD

Khee Trading Recalls Frozen Oysters Due to Norovirus Risk

Khee Trading Inc. recalled 7,306 cases of Frozen Half Shell Oysters on January 27, 2026. The oysters may be contaminated with Norovirus, posing a serious health risk. Consumers should not consume the product and seek a refund or replacement.

Khee Trading
Imported oysters
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Food & Beverages
HIGH
FDA FOOD

Beacon Promotions Recalls M&Ms Over Undeclared Allergens

Beacon Promotions recalled 5,788 units of repackaged M&Ms candies on January 26, 2026. The candies contain undeclared allergens, specifically milk, soy, and peanuts. Consumers should not consume these products and should seek refunds.

Beacon Promotions
Undeclared allergens
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Health & Personal Care
HIGH
FDA DRUG

Asteria Health Recalls Testosterone Pellets Due to Metal Contamination

Asteria Health recalled 1,464 testosterone pellets on January 26, 2026, due to potential metal particulate contamination. The recall affects products distributed nationwide. Consumers must stop using the product immediately and seek guidance from healthcare providers.

F.H. INVESTMENTS, Inc.
Presence of
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Health & Personal Care
HIGH
FDA DRUG

Asteria Health Recalls Estradiol Pellets Due to Metal Contamination

Asteria Health recalled 133 estradiol pellets on January 26, 2026, after detecting potential metal particulate matter. The recall, classified as Class II, affects pellets with lot number 253000126 and an expiration date of June 9, 2026. Consumers must stop using the product immediately and contact their healthcare provider for guidance.

F.H. INVESTMENTS, Inc.
Presence of
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Health & Personal Care
HIGH
FDA DRUG

Asteria Health Recalls Testosterone Pellets Over Metal Contamination

Asteria Health recalled 60,868 testosterone pellets on January 26, 2026, due to contamination risks. The recall affects specific lots of the product that may contain metal particulate matter. Consumers must stop using the product immediately and seek guidance from healthcare providers.

F.H. INVESTMENTS, Inc.
Presence of
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Health & Personal Care
HIGH
FDA DRUG

Asteria Health Recalls Testosterone Pellets Over Metal Contamination Risk

Asteria Health recalled 1,015 testosterone pellets on January 26, 2026 due to potential metal particulate contamination. The recall affects products distributed nationwide in the United States. Consumers must stop using the pellets immediately and contact their healthcare provider for guidance.

F.H. INVESTMENTS, Inc.
Presence of
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Health & Personal Care
HIGH
FDA DRUG

Asteria Health Recalling Estradiol Pellets Due to Metal Contamination

Asteria Health recalled 22,478 Estradiol 12.5 mg pellets on January 26, 2026, due to potential metal particulate contamination. Consumers and healthcare providers must stop using the product immediately. The FDA classified this recall as Class II, indicating a high hazard level.

F.H. INVESTMENTS, Inc.
Presence of
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    chemical hazard Recalls | RecallRadar