adult product Recalls

915 recalls tagged with “adult product”.

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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Health & Personal Care
HIGH
FDA DEVICE

Paradise Renal Denervation Catheter Recalled for 1 Unit in 2026

Paradise Renal Denervation Catheter was recalled after a single unit distributed nationwide in nine states was deemed nonconforming and not for human use. The device is an ultrasound renal denervation catheter. Healthcare providers should stop using it and contact ReCor Medical for instructions.

Paradise
Due to
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Health & Personal Care
HIGH
FDA DRUG

Teva Metoprolol Succinate 200 mg Recall Affects 19,056 Bottles Nationwide (2026)

Teva Pharmaceuticals recalled 19,056 bottles of Metoprolol Succinate Extended-Release Tablets, 200 mg, sold nationwide. The recall cites failed dissolution specifications, which could affect how the drug releases in the body. Patients should stop using the product and contact Teva or their healthcare provider for guidance.

METOPROLOL SUCCINATE
Failed Dissolution
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Health & Personal Care
HIGH
FDA DRUG

Teva Metoprolol Succinate 25 mg Recall for 18,780 Bottles Nationwide in 2026

Teva Pharmaceuticals is recalling 18,780 bottles of Metoprolol Succinate Extended-Release Tablets, 25 mg, distributed nationwide. The recall is due to failed dissolution specifications that could affect dosing. Patients should stop using affected bottles and contact Teva or their healthcare provider for guidance.

Metoprolol Succinate
Failed Dissolution
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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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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 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

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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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 Estradiol Pellets Over Metal Contamination Risk

Asteria Health recalled 50,990 Estradiol pellets on January 26, 2026, due to potential metal particulate matter contamination. The recall affects products distributed nationwide in the USA. Consumers should stop using the pellets 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 Contaminants

Asteria Health recalled 4,599 testosterone pellets on January 26, 2026. The recall follows concerns over potential metal particulate matter contamination. Consumers should 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 Due to Contamination Risk

Asteria Health recalled 62,581 testosterone pellets on January 26, 2026, due to potential metal particulate contamination. Consumers should stop using the product immediately and contact their healthcare provider for guidance. The recall affects testosterone pellets with specific lot numbers and expiration dates.

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 153,498 testosterone pellets on January 26, 2026, due to potential metal particulate contamination. The recall affects lots expiring between June and September 2026. Consumers and healthcare providers must stop using the product immediately.

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 194,336 testosterone pellets on January 26, 2026 due to potential metal contamination. Consumers must stop using the product immediately and contact their healthcare providers. The recall affects nationwide distribution in the USA.

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

Asteria Health Recalls Testosterone Pellets Due to Metal Contamination

Asteria Health recalled 1,758 testosterone pellets on January 26, 2026, due to potential metal particulate contamination. The recall affects pellets distributed nationwide in the USA. Consumers should stop using the product immediately and contact their healthcare providers for guidance.

F.H. INVESTMENTS, Inc.
Presence of
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Tag Statistics

Total Recalls
915

Related Tags

electrical hazardchemical hazardinfant productsuffocation riskstop use immediatelyreturn for refundfda regulatedcpsc regulatedimmediate actionreplacement availableworkplaceplastic