All Product Recalls

Browse through 2,970 product recalls and safety alerts. Filter by hazard level, status, or search for specific products.

Recalled VR Plus and VT Series Vesta Water Heaters
CRITICAL
CPSC

VESTA.DS Recalls VST Tankless Water Heaters for CO Poisoning Hazard (2025)

VESTA.DS recalled VST-brand residential tankless water heaters sold nationwide through retailers after the potential carbon monoxide poisoning hazard was identified. The exhaust duct can crack, letting gases escape into homes and potentially cause death or serious injury. Stop using the recalled water heater and contact VESTA.DS for a free repair; if you must continue using it, install working烟雾与一

VESTA.DS
The exhaust
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Recalled Yamaha Drive 2 J0D/J0E/J5C
HIGH
CPSC

Yamaha Recalls 2021-2025 Drive 2 Golf Cars for Crash Hazard With No Stop Lights

Yamaha recalls 2021-2025 Drive 2 PTV golf cars sold by Yamaha dealers nationwide between June 2020 and July 2025. The recalled golf cars lack stop lights, creating a crash hazard that could result in serious injury or death. Owners should stop using the recalled golf car immediately and contact an authorized Yamaha Golf Car dealer for a free installation of two stoplights.

Yamaha
The recalled
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Recalled DR2A and DR2E Golf Cars
HIGH
CPSC

Yamaha Recalls 2017-2024 Golf Cars Over Brake Failure Crash Hazard (2025)

Yamaha recalled model year 2017-2024 DR2A and DR2E Personal Transportation Vehicles sold through Yamaha dealers nationwide from June 2018 through July 2025. The brake system may fail to engage, creating a crash hazard with potential for serious injury or death. Owners should stop using the recalled golf cars and contact an authorized Yamaha Golf Car dealer to arrange a free brake repair. Yamaha or

Yamaha
The recalled
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Health & Personal Care
HIGH
FDA DEVICE

Beckman Coulter Recalls Bicarbonate Reagent Over High Result Risk

Beckman Coulter recalled 36,981 bicarbonate reagents on October 14, 2025. The reagent may produce falsely high bicarbonate results due to interference from Lactate Dehydrogenase. Healthcare providers and patients must stop using it immediately.

Beckman Coulter Ireland
Bicarbonate reagent
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Health & Personal Care
HIGH
FDA DEVICE

DERMASENSOR DermaSensor 10101 Diagnostic Device Recalled for 9 of 343 Units (2025)

DermaSensor recalled 343 units of its DermaSensor 10101 diagnostic device distributed to medical practices across several states. The device may not meet specifications, producing incorrect results or delaying referrals for patients with suspicious skin lesions. Health care providers should stop using the device immediately and contact Dermasensor Inc for instructions.

DERMASENSOR
Potential for
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Health & Personal Care
HIGH
FDA DEVICE

Paragon 28 Phantom Fibula Nail Recall 2025 for 20 Units Nationwide

Paragon 28 recalled 20 Phantom Fibula Nails nationwide after finding out-of-spec thread depths. The defect may prevent the nail from mating properly with the mounting bolt. Surgery could be aborted if the implant cannot mate with instrumentation. Hospitals and surgeons should stop using the device immediately and follow recall instructions.

Paragon 28
Fibula nail
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Health & Personal Care
HIGH
FDA DEVICE

MRIMed Recalls Mobile Exam Light Battery Over Overheating Hazard

MRIMed recalled 314 batteries for the SL-110 Mobile Exam Light on October 13, 2025. The batteries can overheat while charging, melting internal components and producing smoke. This recall affects devices distributed in the U.S. and several countries worldwide.

MRIMed
Due to
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Health & Personal Care
HIGH
FDA DEVICE

Thoratec Recalls CentriMag Blood Pump Over Serious Hazard

Thoratec recalled 8,399 CentriMag Blood Pumps on October 10, 2025, due to a significant malfunction risk. The blood pump may not securely lock into the motor, potentially leading to serious health complications. The recall affects models distributed worldwide, including across the United States and several countries.

Thoratec
Acute circulatory
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Health & Personal Care
HIGH
FDA DRUG

Mylan Haloperidol Lactate Injection Recalled Over Labeling Errors

Mylan Institutional LLC recalled 800 vials of Haloperidol Lactate Injection on October 10, 2025, due to incorrect RFID tag labels. The product may pose a risk due to potential mislabeling affecting tracking and administration. Healthcare providers should stop using the product immediately and follow up with Safecor Health for guidance.

HALOPERIDOL LACTATE
Labeling: Not
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Health & Personal Care
HIGH
FDA DRUG

CA Botana Sunscreen Flawless Skin Fluid Tint SPF 50 Recall 2025

CA Botana International recalls Sunscreen Flawless Skin Fluid Tint SPF 50 after CGMP deviations. The recall covers 1,401 tubes distributed to California, Colorado, Florida, Puerto Rico and Washington. Stop using the product and contact CA Botana for guidance.

CA Botana International
CGMP Deviations
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Health & Personal Care
HIGH
FDA DRUG

470 Doctor D. Schwab Controlling Cream Tubes Recalled for CGMP Deviations

Doctor D. Schwab recalled 470 tubes of Controlling Cream after discovering CGMP deviations in production. The cream, which contains benzoyl peroxide, may not meet required safety standards. Consumers should stop using the product immediately and contact CA BOTANA for further guidance.

Doctor D. Schwab
CGMP Deviations
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Health & Personal Care
HIGH
FDA DRUG

Elixir by Coco March Tinted Mineral Sunscreen SPF 50 Recalled for CGMP Deviations

A recall is active for Elixir by Coco March Tinted Mineral Sunscreen SPF 50 amid CGMP deviations. The product is distributed by CA Botana International, Inc. The recall cites CGMP deviations as the hazard and class II designation. Consumers should stop using the product and follow guidance from healthcare providers.

SUNSCREEN
CGMP Deviations
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Health & Personal Care
HIGH
FDA DRUG

Lannett NIACIN ER 1,000 mg Recall Affects 46,848 Bottles Nationwide (2025)

Lannett Company, Inc. recalled 46,848 bottles of NIACIN Extended-release Tablets, 1,000 mg, Rx Only, distributed nationwide. The product failed dissolution specifications. Patients and healthcare providers should stop using it immediately and await recall instructions.

Lannett
Failed Dissolution
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Health & Personal Care
HIGH
FDA DRUG

Sugared+Bronzed Tinted Mineral Sunscreen SPF 50 Recalled for CGMP Deviations (Class II)

Sugared+Bronzed recalled 2,090 tubes of tinted mineral sunscreen distributed to California, Colorado, Florida, Puerto Rico and Washington after CGMP deviations were found. The recall, initiated by CA BOTANA International, is active as of Dec 3, 2025. Consumers should stop using the product immediately and contact the distributor for guidance.

Sugared+Bronzed
CGMP Deviations
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Health & Personal Care
HIGH
FDA DRUG

Gabriel Mineral Sunscreen SPF 50 Recalled for CGMP Deviations in 1617 Tubes

Gabriel Mineral Sunscreen SPF 50 is recalled. The FDA-listed recall number D-0190-2026 covers 1617 tubes distributed to California, Colorado, Florida, Puerto Rico and Washington. The recall cites CGMP deviations as the hazard. Consumers should stop using the product immediately and contact CA Botana International or a healthcare provider for guidance.

Gabriel Mineral Sunscreen
CGMP Deviations
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Health & Personal Care
HIGH
FDA DRUG

Dr. Bump Gel Menthol 5% Recall for 4,890 Bottles Over CGMP Deviations

Dr. Bump Gel Menthol 5% recall covers 4,890 bottles distributed by 1Beauty US LLC to California, Colorado, Florida, Puerto Rico and Washington. The recall is due to CGMP deviations. Stop using the product immediately and contact CA Botana International for guidance.

Dr Bump Gel 4
CGMP Deviations
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Health & Personal Care
HIGH
FDA DRUG

CA Botana Doctor D. Schwab Shimmery Sun Lotion Sunscreen Recall for CGMP Deviations (2025)

CA Botana International recalled 805 tubes of Doctor D. Schwab Shimmery Sun Lotion Sunscreen SPF 30 after CGMP deviations were identified. The recall covers tubes sold in California, Colorado, Florida, Puerto Rico, and Washington. Consumers should stop using the product immediately and contact the company for guidance.

Doctor D. Schwab
CGMP Deviations
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