🏨

Other Medical Devices

🏥 Medical Devices 15,203 recalls

Non-medical laser products which were determined to not be in compliance with 21 C.F.R. ¿ 1010.2 in that they currently do not bear the required certification label.

Apr 17, 2024 Other Medical Devices Nationwide View Details →
Class I - Dangerous

The g-MDU (global Mains Distribution Unit) L3 terminal connection may become loose creating a hotspot that may cause smoke/fire to alarm in the hospital's technical room, resulting in Smoke and/or fire

May 3, 2024 Other Medical Devices Nationwide View Details →
Class I - Dangerous

The g-MDU (global Mains Distribution Unit) L3 terminal connection may become loose creating a hotspot that may cause smoke/fire to alarm in the hospital's technical room, resulting in Smoke and/or fire

May 3, 2024 Other Medical Devices Nationwide View Details →

Issue related to Novalung sensor box, which is a component of the Novalung Console (Part Number F30000163). In certain instances, error messages #206 (yellow) and #208 (red) technical failure, flow measurement during use of the Novalung system.

Apr 8, 2024 Other Medical Devices Nationwide View Details →

Products have a lack of sterility assurance.

Mar 12, 2024 Other Medical Devices Nationwide View Details →

Potential for unsealed sterile packing.

Mar 19, 2024 Other Medical Devices View Details →