🏥 Medical Devices Class I - Dangerous
There is potential for packaging defects that may impact the sterile barrier.
All Recalls
95,018 total recalls in our database
10 ga ARS Decompression Needle, Part Number ZZ-0298
North American Rescue
🏥 Medical Devices Class I - Dangerous
The device includes the incorrect Instructions for Use.
General Manual surgical instrument
M.D.L. S.r.l.
🏥 Medical Devices Class I - Dangerous
Sterility assurance may be compromised.
🏥 Medical Devices Class I - Dangerous
Malfunction- loosening of the implant resulting in a potential revision surgery
🏥 Medical Devices Class I - Dangerous
There is potential for packaging defects that may impact the sterile barrier.
Catalog A902916, SureStep" Foley Tray, Lubricath", Urine Meter, StatLock" Stabilization Device
C.R. Bard
🏥 Medical Devices Class I - Dangerous
There is potential for packaging defects that may impact the sterile barrier.
🏥 Medical Devices Class I - Dangerous
Due to a software defect that can intermittently cause the system to lock-up which exiting Review Mode while performing an exam.
🏥 Medical Devices Class I - Dangerous
Ultrasound gels and lotions manufactured by Eco-Med Pharmaceutical, Inc. may contain bacterial contamination.
Aspirated Cyto-Histological Biopsy needle
M.D.L. S.r.l.
🏥 Medical Devices Class I - Dangerous
Sterility assurance may be compromised.
🏥 Medical Devices Class I - Dangerous
There is potential for packaging defects that may impact the sterile barrier.
Bone Marrow Transplantation biopsy needle
M.D.L. S.r.l.
🏥 Medical Devices Class I - Dangerous
Sterility assurance may be compromised.
🏥 Medical Devices Class I - Dangerous
Due to a software defect that can intermittently cause the system to lock-up which exiting Review Mode while performing an exam.
🏥 Medical Devices Class I - Dangerous
Complaints were received of CoLink Bone Graft Harvesters breaking at the outer tube weld site.
🏥 Medical Devices Class I - Dangerous
There is potential for packaging defects that may impact the sterile barrier.
🏥 Medical Devices Class I - Dangerous
Malfunction- loosening of the implant resulting in a potential revision surgery
🏥 Medical Devices Class I - Dangerous
Malfunction- loosening of the implant resulting in a potential revision surgery
🏥 Medical Devices Class I - Dangerous
Malfunction- loosening of the implant resulting in a potential revision surgery
🏥 Medical Devices Class I - Dangerous
Firm's submission for Emergency Use Authorization (EUA) contained insufficient evidence to be granted EUA Authorization to distribute
🏥 Medical Devices Class I - Dangerous
There is potential for packaging defects that may impact the sterile barrier.
🏥 Medical Devices Class I - Dangerous
There is potential for packaging defects that may impact the sterile barrier.