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Medical Devices Recalls

Medical equipment, implants, and diagnostic devices

38,779 Total Recalls

The wrong instructions for use (IFU) were supplied with the AnastoClip GC closure system. The IFU provided lists some indications which are not cleared by the FDA for devices distributed in the United States: 1) closure of arteriotomies and veinotomies, 2) attachment of synthetic vascular prostheses, and 3) approximation of dural tissue.

Jun 19, 2018 Other Medical Devices View Details →

The care-e-vac(R)3 Battery/AC Powered Portable Aspirator battery terminal may come in contact with the pump causing an electric short leading to damage to wiring and resulting in loss of function or an inoperable unit under battery power.

Aug 14, 2018 Infusion Pumps Nationwide View Details →