Recalls of medical devices, diagnostic equipment, implants, and surgical instruments.
Showing 601–620 of 1,000 recalls
Smiths Medical ASD, Inc.
The plastic port housing and port reservoir of the ProPort Plastic Implantable Ports may separate because of a manufacturing defect.
Medtronic Perfusion Systems
Unexpected loose material in the male luer used in the aortic root cannula has been identified. Potential harms when identified prior to use - procedure delay. Potential harm if not identified and used - stroke (reversible and irreversible).