stop use immediately Recalls

1,862 recalls tagged with “stop use immediately”.

Health & Personal Care
HIGH
FDA DEVICE

ReCor Medical Paradise Ultrasound Renal Denervation System Recall 2026: 24 Catheters PRDS-068-02

ReCor Medical Inc. has issued an active recall for 24 Paradise ultrasound renal denervation catheters distributed nationwide in nine states. The devices were nonconforming and were supposed to be scrapped and not for human use. Healthcare providers and patients should stop using the devices immediately and await manufacturer recall instructions.

ReCor Medical
Due to
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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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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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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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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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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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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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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 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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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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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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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

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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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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Tag Statistics

Total Recalls
1,862

Related Tags

fda regulatedimmediate actionreturn for refundnhtsa regulatedreplacement availableadult productchoking hazardinfant productcpsc regulatedpoisoning riskchildren productelectrical hazard