stop use immediately Recalls

Olympus Thunderbeat Surgical Instrument Recalled Due to Safety Concerns

Firm is initiating a removal due to continued reports of adverse events.

Olympus Thunderbeat Surgical Device Recalled Over Adverse Events

Firm is initiating a removal due to continued reports of adverse events.

Olympus Thunderbeat Surgical Device Recalled Due to Hazardous Events

Firm is initiating a removal due to continued reports of adverse events.

Olympus Thunderbeat Device Recalled Due to Adverse Events

Firm is initiating a removal due to continued reports of adverse events.

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 Thunderbeat Surgical Device Recalled Due to Adverse Events

Firm is initiating a removal due to continued reports of adverse events.

Olympus Thunderbeat Surgical Device Recalled Due to Adverse Events

Firm is initiating a removal due to continued reports of adverse events.

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

Lack of Assurance of Sterility.

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

Mindray DS USA Recalls 54 Isoflurane V90 Vaporizers for A9 Anesthesia System Over Leakage Risk (2025

Mindray Sevoflurane V90 Vaporizer Recalled for Leakage Risk in A9 System (148 Units)

Mindray DS USA recalled 148 Sevoflurane V90 electronic vaporizers used with the A9 Anesthesia System. The devices have a potential for anesthesia leakage. Healthcare facilities should stop using the device immediately and follow manufacturer instructions.

123Herbals SILINTAN 25-Pill Meloxicam Recall in 2026

Marketed Without an Approved NDA/ANDA: FDA analysis revealed the presence of undeclared meloxicam.

Town Food Service Recalls Aluminum Sauce Pans Over Lead Hazard

Product found to contain leachable lead levels.

Straumann USA Recalls 61 Emdogain Demonstration Dental Devices (2025)

The possibility for this product that is intended for demonstration purposes only to be placed in patients.

RH Byron Tables and Desks Recalled for Injury Risk — 31 SKUs in 2025

WLIVE Fabric 12-Drawer Dressers Recalled for Tip-Over Risk (2025)

AOWOS 12-Drawer Dressers Recalled for Tip-Over Hazard — Check Model Numbers

Super Wheels Vaast A/1 Bicycle and Frameset Recall 2025 for 35 Bikes and 15 Framesets

DEVI Cinnamon Powder Recall: 140 Packets in WA for Lead Contamination (2025)

Elevated levels of lead. FDA ground cinnamon sample was found to contain 2.92 mg/kg.

Nat's Nuts Cinnamon Whiskey Pecans Recalled for Undeclared Cashews in 600 Units (2025)

Nat's Nuts LLC recalled 600 units of Cinnamon Whiskey Pecans sold through multiple retailers. The recall is due to undeclared cashews, creating an allergy risk. Stop using the product and contact Nat's Nuts LLC for refund or replacement information.