stop use immediately Recalls

2,153 recalls tagged with “stop use immediately”.

Recalled Pack-N-Stroll Premium Folding Utility Wagon
HIGH
CPSC

Olympia Tools Recalls Pack-N-Stroll Premium Folding Utility Wagon for 2025 Entrapment and Falls Risk

Olympia Tools International recalls Pack-N-Stroll Premium Folding Utility Wagons sold at Costco after authorities determined the product can trap a child’s head and cause serious injury or death. The defect is an opening between the organizational tray and the sidewall. The wagon also lacks a restraint system. Stop using the wagon now and return it to Costco for a full refund.

Olympia Tools International
The utility
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Recalled Cranach Hardware Plastic Tip Restraint Kit
HIGH
CPSC

Cranach Hardware Recalls Tip Restraint Kits for Tip-Over Hazard (2025)

No injuries have been reported. Cranach Hardware recalled tip restraint kits sold through retailers after testing showed the plastic brackets and tie can fail to meet safety standards. Stop using the restraints and contact Cranach Hardware for a free stainless steel replacement kit.

Cranach Hardware
The recalled
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Recalled Lifepro Sauna Blanket
HIGH
CPSC

Lifepro Bioremedy Infrared Sauna Blankets Recalled for Burn Hazard (2025)

Lifepro Fitness recalls Bioremedy Infrared Sauna Blankets sold with gray-faced controllers due to burn risk. The recall affects models LP-BRMDYL-BLK, LP-BRMDYL-GRY, LP-BRMDYR-BLK, LP-BRMDYR-GRY, LP-BRMDYR-BLU, LP-BRMDYR-PNK, and LP-BRMDYR-PRPL. Consumers should stop using and unplug the blankets and visit Lifepro’s recall page for a replacement.

Lifepro Fitness
The sauna
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Health & Personal Care
HIGH
FDA DEVICE

Olympus Thunderbeat Surgical Device Recalled Over Adverse Events

Olympus Corporation of the Americas recalled the Thunderbeat 5 mm, 35 cm, Front-Actuated Grip on October 22, 2025. The recall follows reports of adverse events associated with the device. Healthcare providers and patients must stop using this product immediately.

Olympus Corporation of the Americas
Firm is
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Health & Personal Care
HIGH
FDA DEVICE

Olympus Thunderbeat Surgical Device Recalled Due to Hazardous Events

Olympus Corporation of the Americas recalled the Thunderbeat, 5 mm, 45 cm, Pistol Grip device on October 22, 2025. The recall affects 30 units distributed worldwide, including the U.S., Canada, Brazil, Germany, Mexico, and Japan. Patients and healthcare providers must stop using this device immediately due to reports of adverse events.

Olympus Corporation of the Americas
Firm is
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Health & Personal Care
HIGH
FDA DEVICE

Olympus Thunderbeat Device Recalled Due to Adverse Events

Olympus Corporation of the Americas recalled the Thunderbeat 5 mm, 20 cm, Front-Actuated Grip on October 22, 2025. The recall follows ongoing reports of adverse events associated with the medical device. Patients and healthcare providers must stop using the device immediately and follow recall instructions.

Olympus Corporation of the Americas
Firm is
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Health & Personal Care
HIGH
FDA DEVICE

Olympus Thunderbeat Surgical Instrument Recalled Due to Safety Concerns

Olympus Corporation of the Americas recalled the Thunderbeat, 5 mm, 45 cm Front-Actuated Grip on October 22, 2025. The recall follows ongoing reports of adverse events associated with the device. Healthcare providers and patients must stop using the instrument immediately.

Olympus Corporation of the Americas
Firm is
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Health & Personal Care
HIGH
FDA DEVICE

Olympus Recalls Thunderbeat Surgical Instrument Over Safety Concerns

Olympus Corporation of the Americas recalled 9,542 units of the Thunderbeat 5 mm, 45 cm, Front-Actuated Grip Type S on October 22, 2025. The recall follows continued reports of adverse events associated with the device. Patients and healthcare providers must stop using it immediately and follow manufacturer instructions.

Olympus Corporation of the Americas
Firm is
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Health & Personal Care
HIGH
FDA DEVICE

Olympus Thunderbeat Surgical Device Recalled Over Safety Concerns

Olympus Corporation of the Americas recalled 1,538 units of the Thunderbeat 5 mm, 10 cm, Inline Grip on October 22, 2025. The recall follows multiple reports of adverse events linked to the device. Healthcare providers and patients should stop using it immediately and follow the manufacturer's instructions.

Olympus Corporation of the Americas
Firm is
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Health & Personal Care
HIGH
FDA DEVICE

Olympus Thunderbeat Surgical Device Recalled Over Adverse Events

Olympus Corporation of the Americas recalled the Thunderbeat surgical device on October 22, 2025, due to reports of adverse events. The recall affects 30 units distributed worldwide, including the US, Canada, and Japan. Patients and healthcare providers must stop using the device immediately.

Olympus Corporation of the Americas
Firm is
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Health & Personal Care
HIGH
FDA DEVICE

Olympus Thunderbeat Surgical Device Recalled Due to Adverse Events

Olympus Corporation of the Americas recalled 88,268 units of the Thunderbeat surgical device on October 22, 2025. The recall follows reports of adverse events associated with the device. Healthcare providers and patients should stop using the device immediately and follow the recall instructions.

Olympus Corporation of the Americas
Firm is
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Health & Personal Care
HIGH
FDA DEVICE

Olympus Thunderbeat Surgical Device Recalled Due to Adverse Events

Olympus Corporation of the Americas recalled 140 units of its Thunderbeat surgical device on October 22, 2025. Users reported ongoing adverse events linked to the device. Healthcare providers should stop using it immediately and follow recall instructions.

Olympus Corporation of the Americas
Firm is
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Health & Personal Care
HIGH
FDA DEVICE

Olympus Thunderbeat Surgical Device Recalled Due to Adverse Events

Olympus Corporation of the Americas recalled 52 units of the Thunderbeat, 5 mm, 35 cm, Inline Grip on October 22, 2025. Reports of adverse events prompted the removal of this medical device from the market. The recall affects distribution in the US, Brazil, Canada, Germany, Mexico, and Japan.

Olympus Corporation of the Americas
Firm is
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Health & Personal Care
HIGH
FDA DEVICE

Olympus Thunderbeat Surgical Instrument Recalled Due to Hazards

Olympus Corporation recalled 3,381 units of the Thunderbeat surgical instrument on October 22, 2025. The recall follows continued reports of adverse events associated with the device. Patients and healthcare providers must stop using the product immediately.

Olympus Corporation of the Americas
Firm is
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Health & Personal Care
HIGH
FDA DRUG

Bristol-Myers Squibb Opdualag Vial Recall for Sterility Risk: 12,778 Units (2025)

Bristol-Myers Squibb recalled 12,778 Opdualag single-dose vials nationwide after a lack of assurance of sterility was identified. The product is nivolumab and relatlimab-rmbw injection. The recall date is 2025-10-21. Healthcare providers should stop using affected lots and follow the recall letter guidance.

Opdualag
Lack of
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Health & Personal Care
HIGH
FDA DEVICE

Medtronic MiniMed CareLink Clinic Recall 12,126 Units Worldwide in 2025

Medtronic MiniMed recalled 12,126 CareLink Clinic units worldwide after a software error misdisplays the 24-hour Sensor Glucose Overview Graph. The faulty software could prompt clinicians and patients to make therapy decisions based on incorrect glucose data. Patients should stop using the device immediately and contact Medtronic MiniMed or their healthcare provider for instructions.

Medtronic MiniMed
Software error
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Health & Personal Care
CRITICAL
FDA DRUG

123Herbals SILINTAN 25-Pill Meloxicam Recall in 2026

123Herbals LLC recalled SILINTAN 25-pill bottles sold nationwide in the United States after FDA analysis found undeclared meloxicam. An NDA/ANDA violation is cited. Consumers and healthcare providers should stop using this product immediately and contact 123Herbals LLC for guidance.

123Herbals
Marketed Without
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Tag Statistics

Total Recalls
2,153

Related Tags

infant productchildren productoutdoorplasticmetalreturn for refundmandatory standard violationnhtsa regulatedcpsc regulatedreplacement availablerepair availableimmediate action