AVID Medical, Inc. recalls Halyard ORGAN RECOVERY OR PACK
Devices are not suitable for organ transplant.
Drawn from openFDA device enforcement reports. Filter by severity, status, state, year, or manufacturer.
Showing 253–264 of 634 recalls
Devices are not suitable for organ transplant.
Devices are not suitable for organ transplant.
Ophthalmic procedure packs may have incomplete seals affecting sterility.
A certain component of affected devices was not delivered within specification and contained impurities.
A certain component of affected devices was not delivered within specification and contained impurities.
Potential unexpected shutdown of Carestation 600 and 700 Series Anesthesia Systems containing certain power management boards, if the AC mains power is unplugged or in the event of an AC mains power failure.…
Potential unexpected shutdown of Carestation 600 and 700 Series Anesthesia Systems containing certain power management boards, if the AC mains power is unplugged or in the event of an AC mains power failure.…
Potential unexpected shutdown of Carestation 600 and 700 Series Anesthesia Systems containing certain power management boards, if the AC mains power is unplugged or in the event of an AC mains power failure.…
Software version 5.10.1 and earlier contain anomalies that have the potential to cause serious patient harm or death.
Multiple complaints were reported in which cracks formed in the hose of specific catheter mounts.
Multiple complaints were reported in which cracks formed in the hose of specific catheter mounts.
Multiple complaints were reported in which cracks formed in the hose of specific catheter mounts.