All Product Recalls

Browse through 2,959 product recalls and safety alerts. Filter by hazard level, status, or search for specific products.

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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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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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 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

Lutronic CLARITY II Laser System Recalled for 1,525 Units Worldwide in 2026

Lutronic's CLARITY II Laser System, 1,525 units distributed worldwide to US clinics and international markets, is recalled. The devices have reports of sparking and popping during use and may burn patients. Clinics and patients should stop using the device immediately and follow the manufacturer's recall instructions.

Lutronic
Reports of
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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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Health & Personal Care
HIGH
FDA DEVICE

Abiomed Impella RP Recall 179 Units for Sensor Drift Risk (2026)

Abiomed recalled 179 Impella RP devices worldwide after a differential pressure sensor may drift. The fault can cause sensor values to drift, potentially affecting patient care. Stop using the device immediately and follow the recall instructions, including contacting Abiomed or your healthcare provider.

Abiomed
Differential pressure
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Health & Personal Care
HIGH
FDA DEVICE

Abiomed Impella RP with SmartAssist Recall Affects 291 Units Worldwide in 2026

Abiomed recalled 291 Impella RP with SmartAssist devices sold worldwide, including the US. A differential pressure sensor may malfunction and cause readings to drift. Patients and healthcare providers should stop using the device immediately and follow the manufacturer’s recall instructions.

Abiomed
Differential pressure
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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 DEVICE

Philips Medical Systems Recalls Azurion 3 M12 Due to Hazard

Philips Medical Systems recalled 291 Azurion 3 M12 systems on January 26, 2026, due to a risk of unexpected table movement. This may occur when the Reset Geometry button is pressed, even if a table lock is active. The recall affects 27 units in the U.S. and 264 units internationally.

PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.
Under certain
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Health & Personal Care
HIGH
FDA DEVICE

Philips Medical Systems Recalls Azurion 7 B12 Table Due to Safety Risk

Philips Medical Systems Netherlands B.V. recalled 655 Azurion 7 B12 systems on January 26, 2026. The recall affects models 722067, 722225, and 722235 due to unexpected table movement when the Reset Geometry button is pressed. This poses a high risk of injury to patients and healthcare providers.

PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.
Under certain
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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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