All Recalls

95,018 total recalls in our database

πŸ₯ Medical Devices Class I - Dangerous

An increased number of complaints were reported on the Blood Pump Rotor (P/N - F40015481 REV A) after a period of use by clinics noting loose/dislodged guide sheaves.

Apr 17, 2024 Infusion Pumps Nationwide View Details β†’
πŸ₯ Medical Devices Class I - Dangerous

Potential for devices to experience interruption/loss of therapy during a Ventilator Inoperative alarm. This may lead to hypoventilation, mild to severe hypoxemia, hypercarbia, respiratory failure/insufficiency, or potentially death in the most vulnerable patients.

Mar 26, 2024 Patient Monitors Nationwide View Details β†’

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 Diagnostic Equipment Nationwide View Details β†’