All Recalls

95,083 total recalls in our database

🏥 Medical Devices Class I - Dangerous

Zimmer Biomet Inc. initiated a field action on 02/28/2017 for sterile-packaged implants packaged in two different package configurations due to packaging design verification test failures.

Feb 28, 2017 Other Medical Devices Nationwide View Details →

Philips DigitalDiagnost 3.1.x X-Ray System

Philips Electronics North America

🏥 Medical Devices Class I - Dangerous

During recent evaluations of the Philips DigitalDiagnost 3.1.x, we have identified a potential issue that may affect the performance of the equipment under certain conditions.

May 11, 2017 Other Medical Devices Nationwide View Details →
🏥 Medical Devices Class I - Dangerous

reprocessing instructions do not provide sufficient detailed information for the cleaning, disinfection, and sterilization of these products

Apr 25, 2017 Other Medical Devices Nationwide View Details →
🏥 Medical Devices Class I - Dangerous

reprocessing instructions do not provide sufficient detailed information for the cleaning, disinfection, and sterilization of these products

Apr 25, 2017 Surgical Instruments Nationwide View Details →