DeRoyal TOTAL HIP KIT, REF 89-9498.08
DeRoyal Industries
🏥 Medical Devices Class I - Dangerous
XXX
All Recalls
95,018 total recalls in our database
STRADIS HEALTHCARE, PROBE COVER W/GEL PACK, Item No.525-071, general surgery tray
Stradis Medical, LLC
🏥 Medical Devices Class I - Dangerous
Medical and surgical procedure trays and kits underwent certain manufacturing conditions that may result in the outer bag being incompletely sealed, which may result in a breach in the sterility of the kit.
DeRoyal HEART PACK, REF 89-8351.11
DeRoyal Industries
🏥 Medical Devices Class I - Dangerous
XXX
DeRoyal SHOULDER PACK, REF 89-6830.13
DeRoyal Industries
🏥 Medical Devices Class I - Dangerous
XXX
DeRoyal ENDOVENOUS PACK, REF 89-7762.05
DeRoyal Industries
🏥 Medical Devices Class I - Dangerous
DeRoyal procedure packs that contain the affected 3M Health Care Steri Drapes which have been recalled.
STRADIS HEALTHCARE, SAFETY PINS, SMALL 1" Item No.515-001
Stradis Medical, LLC
🏥 Medical Devices Class I - Dangerous
Medical and surgical procedure trays and kits underwent certain manufacturing conditions that may result in the outer bag being incompletely sealed, which may result in a breach in the sterility of the kit.
DeRoyal CUSTOM NEURO PACK, REF 89-8392.09
DeRoyal Industries
🏥 Medical Devices Class I - Dangerous
DeRoyal procedure packs that contain the affected 3M Health Care Steri Drapes which have been recalled.
DeRoyal BIOPSY PACK, REF 89-9270.05
DeRoyal Industries
🏥 Medical Devices Class I - Dangerous
XXX
DeRoyal BASIC NEURO PACK, REF 89-7258.13
DeRoyal Industries
🏥 Medical Devices Class I - Dangerous
DeRoyal procedure packs that contain the affected 3M Health Care Steri Drapes which have been recalled.
DeRoyal EYE PACK, REF 89-4051.09
DeRoyal Industries
🏥 Medical Devices Class I - Dangerous
DeRoyal procedure packs that contain the affected 3M Health Care Steri Drapes which have been recalled.
DeRoyal CATARACT PACK, REF 89-10086.05
DeRoyal Industries
🏥 Medical Devices Class I - Dangerous
DeRoyal procedure packs that contain the affected 3M Health Care Steri Drapes which have been recalled.
Arrow AutoCAT2 Intra-Aortic Balloon Pump, AUTOCAT2 WAVE REFURBISHED, REF IAP-0500X (IPN000328), cardiac pump
ARROW INTERNATIONAL
🏥 Medical Devices Class I - Dangerous
There is a potential issue with short battery run-times on the affected intra-aortic balloon pump (IABP) devices.
DeRoyal LAPINECTOMY PACK, REF 89-7198.10
DeRoyal Industries
🏥 Medical Devices Class I - Dangerous
XXX
🏥 Medical Devices Class I - Dangerous
There is a potential issue resulting in the Power Supply potentially becoming overheated due to internal components overstressing. Consequently, due to the overstressing of the internal components, one specific component can fail which will cause the device to unexpectedly shutdown.
GEO-MED PODIATRY PACK PGYBK, REF 89-6240.05
DeRoyal Industries
🏥 Medical Devices Class I - Dangerous
DeRoyal procedure packs that contain the affected 3M Health Care Steri Drapes which have been recalled.
STRADIS HEALTHCARE, Custom Pack, Item No.41213ATCP, dental
Stradis Medical, LLC
🏥 Medical Devices Class I - Dangerous
Medical and surgical procedure trays and kits underwent certain manufacturing conditions that may result in the outer bag being incompletely sealed, which may result in a breach in the sterility of the kit.
DeRoyal NEURO PACK, REF 89-10171.06
DeRoyal Industries
🏥 Medical Devices Class I - Dangerous
XXX
HENRY SCHEIN, BREAST PACK, Item No.570-2397
Stradis Medical, LLC
🏥 Medical Devices Class I - Dangerous
Medical and surgical procedure trays and kits underwent certain manufacturing conditions that may result in the outer bag being incompletely sealed, which may result in a breach in the sterility of the kit.
DeRoyal CRANI PACK, REF 89-10242.04
DeRoyal Industries
🏥 Medical Devices Class I - Dangerous
DeRoyal procedure packs that contain the affected 3M Health Care Steri Drapes which have been recalled.
HENRY SCHEIN, ILR Insertion Tray, Item No.570-3131
Stradis Medical, LLC
🏥 Medical Devices Class I - Dangerous
Medical and surgical procedure trays and kits underwent certain manufacturing conditions that may result in the outer bag being incompletely sealed, which may result in a breach in the sterility of the kit.