Olympus Thunderbeat Surgical Device Recalled Over Adverse Events
Firm is initiating a removal due to continued reports of adverse events.
2,756 recalls tagged with “immediate action”.
Firm is initiating a removal due to continued reports of adverse events.
Firm is initiating a removal due to continued reports of adverse events.
Lack of Assurance of Sterility.
Marketed Without an Approved NDA/ANDA: FDA analysis revealed the presence of undeclared meloxicam.
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.
The possibility for this product that is intended for demonstration purposes only to be placed in patients.
Product found to contain leachable lead levels.

Cooked egg ingredient for Ready-to-Eat products tested positive for Listeria Monocytogenes






Cooked egg ingredient for Ready-to-Eat products tested positive for Listeria Monocytogenes
Elevated levels of lead. FDA ground cinnamon sample was found to contain 2.92 mg/kg.
