DeRoyal SHOULDER KIT, REF 89-9497.10
DeRoyal Industries
🏥 Medical Devices Class I - Dangerous
XXX
All Recalls
95,018 total recalls in our database
DeRoyal GU PACK, REF 89-10665.02
DeRoyal Industries
🏥 Medical Devices Class I - Dangerous
XXX
GEO-MED OPTHALMOLOGY CSTM PCK, REF 89-6387.08
DeRoyal Industries
🏥 Medical Devices Class I - Dangerous
DeRoyal procedure packs that contain the affected 3M Health Care Steri Drapes which have been recalled.
Arrow AutoCAT2WAVE Intra-Aortic Balloon Pump, Arrow AutoCAT2WAVE IABP, REF IAP-0500EX (IPN000322), 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 EMERGENT TRAUMA PACK, ref 89-9453.12
DeRoyal Industries
🏥 Medical Devices Class I - Dangerous
XXX
STRADIS HEALTHCARE, Ablation Pack, Item No.682-130,
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 BASIC PACK, REF 89-8633.07
DeRoyal Industries
🏥 Medical Devices Class I - Dangerous
XXX
Arrow AutoCAT2 Intra-Aortic Balloon Pump, AC3 IABP NA/AJLA, REF IAP-0601 (IPN001109), 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.
HENRY SCHEIN, CUSTOM PK 2, Item No.570-3072
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.
🏥 Medical Devices Class I - Dangerous
Zimmer Biomet is conducting a voluntary medical device recall related to the NexGen Stemmed Option Tibial Components due to the clinically and statistically significant higher overall revision rates when these tibial components are used with either the Legacy Posterior Stabilized (LPS) Flex or LPS Flex Gender Solutions Femoral (GSF) components as compared to other total knee arthroplasties in the United Kingdom National Joint Registry (UK NJR). Removing the NexGen Stemmed Option Tibial Component f rom inventory will prevent its future implantation with either the LPS Flex or LPS Flex GSF femoral components and mitigate the increased revision risk with these two specific combinations of tibial and femoral component.
IMMULITE 2000 Systems 3gAllergy Specific IgE Universal Kit Tests OUS, except Japan Siemens Material Number (SMN): 10380875 For the quantitative measurement of allergen-specific IgE in human serum, as an aid in the clinical diagnosis of IgE mediated allergic disorders.
Siemens Healthcare Diagnostics
🏥 Medical Devices Class I - Dangerous
Potential for falsely elevated specific IgE mold allergen reactivity with quality control material and patient samples, may result in false reactive result
Surgical room, DENTAL SURGICAL PACK, Item No.41236SDSP
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 TOTAL SHOULDER PACK, REF 89-10151.05
DeRoyal Industries
🏥 Medical Devices Class I - Dangerous
XXX
Arrow AutoCAT2WAVE Intra-Aortic Balloon Pump, Arrow AutoCAT2WAVE IABP, REF IAP-0500J (IPN000334), 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 BASIC EYE PACK, REF 89-8337.09
DeRoyal Industries
🏥 Medical Devices Class I - Dangerous
XXX
Arrow AutoCAT2WAVE Intra-Aortic Balloon Pump, Arrow AutoCAT2WAVE IABP, REF IAP-0500I (IPN000324), 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 NEURO PACK, REF 89-9253.09
DeRoyal Industries
🏥 Medical Devices Class I - Dangerous
XXX
🏥 Medical Devices Class I - Dangerous
Suction ports may potentially be occluded on the affected devices. If this occurs, the affected devices will not be able to perform the suction function during use, which could cause a delay in procedure and could require another device to be used.
DeRoyal NEURO PACK, REF 89-10682.02
DeRoyal Industries
🏥 Medical Devices Class I - Dangerous
XXX
DeRoyal SPINAL FUSION PACK, REF 89-7515.14
DeRoyal Industries
🏥 Medical Devices Class I - Dangerous
DeRoyal procedure packs that contain the affected 3M Health Care Steri Drapes which have been recalled.