95,114 total recalls in our database
Ossur Americas
Due to insufficient column strength of the racks for all load conditions, racks associated with height adjustment functionality have been observed deforming, which may lead to increased range of motion in the cervical spine.
Circulatory Technology
The device is used as part of extracorporeal membrane oxygenation (ECMO) cardiopulmonary bypass circuits and may collapse during use which can increase resistance to flow in the venous line and cause a drop in circuit blood flow.
Radiometer Medical ApS
Due to an issue with the internal clock of the analyzers with an e3800 PC unit installed.
Medtronic Perfusion Systems
Specific lots may have been manufactured with insufficient or incomplete welds.
Medtronic Perfusion Systems
Specific lots may have been manufactured with insufficient or incomplete welds.
The product may have a yellowish-brown/greenish-brown residue present at the tip of the cannula.
Medtronic Perfusion Systems
Specific lots may have been manufactured with insufficient or incomplete welds.
Medtronic Perfusion Systems
Specific lots may have been manufactured with insufficient or incomplete welds.
The company was notified by their supplier of sterilization services for airway products in Italy of potential deviations from validated parameters for ethylene oxide sterilization.
Medtronic Perfusion Systems
Specific lots may have been manufactured with insufficient or incomplete welds.
Abbott Laboratories Inc. (St Jude Medical)
Due to a software error, the user may lose functionality of the system or the screen may turn black during operation.
Medtronic Perfusion Systems
Specific lots may have been manufactured with insufficient or incomplete welds.
Medtronic Perfusion Systems
Specific lots may have been manufactured with insufficient or incomplete welds.
Medtronic Perfusion Systems
Specific lots may have been manufactured with insufficient or incomplete welds.
Medtronic Perfusion Systems
Specific lots may have been manufactured with insufficient or incomplete welds.
Reports of the proximal end of the stent not immediately expanding upon deployment and remaining connected to the delivery system.
Abbott Laboratories Inc. (St Jude Medical)
Due to a software error, the user may lose functionality of the system or the screen may turn black during operation.
Skytron, Div. The KMW Group
Failure of the FS32 Monitor Brackets from the mounting block could potentially loosen over time and eventually detach from the baseplate, result in the display interface dismounting from its attachment point, causing injury to patients or staff
Medtronic Perfusion Systems
Specific lots may have been manufactured with insufficient or incomplete welds.
Angio tubing included within Custom Convenience kits may contain insufficient or incomplete weld