Medical DeviceDec 21, 2022
DeRoyal KIT TOTAL HIP, REF 89-8861.07 recall — FDA Z-0627-2023
DeRoyal procedure packs that contain the affected 3M Health Care Steri Drapes which have been recalled.
Class IIFDA: OngoingDeRoyal Industries Inc.
Latest records
Latest recalls — page 644
The newest recall records with useful source details are listed here.
Medical DeviceDec 21, 2022
Stradis Medical, LLC dba Stradis Healthcare HENRY SCHEIN, BASIC EXTENDED PACK, Item recall — FDA Z-0521-2023
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…
Class IIFDA: OngoingStradis Medical, LLC dba Stradis Healthcare
Medical DeviceDec 21, 2022
Stryker Medical Division of Stryker Power-PRO 2, Model No. 6507, Item No. 650705550001 (US) recall — FDA Z-0479-2023
Cot may experience unintended motion due to damaged cables. Potential risk of soft tissue injury to patients such as scrapes or bruises resulting from the cot lowering faster than expected.
Class IIFDA: OngoingStryker Medical Division of Stryker Corporation
Medical DeviceDec 21, 2022
STRADIS HEALTHCARE, Surg, Item No.40551TMS. oral surgery tray recall — FDA Z-0487-2023
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…
Class IIFDA: OngoingStradis Medical, LLC dba Stradis Healthcare
Medical DeviceDec 21, 2022
STRADIS HEALTHCARE, Endo Pack, Item No.682-509 recall — FDA Z-0550-2023
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…
Class IIFDA: OngoingStradis Medical, LLC dba Stradis Healthcare
Medical DeviceDec 21, 2022
Zimmer NexGen Option Stemmed Tibial Component Size 4, Item Number 00-5986-037-02 recall — FDA Z-0467-2023
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…
Class IIFDA: OngoingZimmer, Inc.
Medical DeviceDec 21, 2022
Zimmer NexGen Option Stemmed Tibial Component Size 5, Item Number 00-5986-047-01 recall — FDA Z-0468-2023
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…
Class IIFDA: OngoingZimmer, Inc.
Medical DeviceDec 21, 2022
Stradis Medical, LLC dba Stradis Healthcare HENRY SCHEIN, EXTREMITY PACK, Item No.570-2946 recall — FDA Z-0526-2023
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…
Class IIFDA: OngoingStradis Medical, LLC dba Stradis Healthcare
Medical DeviceDec 21, 2022
DeRoyal SPINAL FUSION PACK, REF 89-7515.12 recall — FDA Z-0596-2023
DeRoyal procedure packs that contain the affected 3M Health Care Steri Drapes which have been recalled.
Class IIFDA: OngoingDeRoyal Industries Inc.
Medical DeviceDec 21, 2022
DeRoyal EYE TRAY, REF 89-4957.08 recall — FDA Z-0564-2023
DeRoyal procedure packs that contain the affected 3M Health Care Steri Drapes which have been recalled.
Class IIFDA: OngoingDeRoyal Industries Inc.
Medical DeviceDec 21, 2022
Allison Medical CarePoint 60 mL Syringe Without Needle, REF: 04-7560 recall — FDA Z-0478-2023
Syringe without needle may have a green substance on the plunger. Substance found to be nontoxic but its effect on drug potency or interaction is unknown.
Class IIFDA: CompletedAllison Medical, Inc.
Medical DeviceDec 21, 2022
Stradis Medical, LLC dba Stradis Healthcare www.StradisHealthcare.com, Endovenous Pack, Item recall — FDA Z-0549-2023
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…
Class IIFDA: OngoingStradis Medical, LLC dba Stradis Healthcare
Medical DeviceDec 21, 2022
DeRoyal MAJOR ORAL PACK RF, REF 89-3936.15 recall — FDA Z-0561-2023
DeRoyal procedure packs that contain the affected 3M Health Care Steri Drapes which have been recalled.
Class IIFDA: OngoingDeRoyal Industries Inc.
Medical DeviceDec 21, 2022
Stradis Medical, LLC dba Stradis Healthcare HENRY SCHEIN, MAJOR EXTREMITY PACK, Item recall — FDA Z-0516-2023
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…
Class IIFDA: OngoingStradis Medical, LLC dba Stradis Healthcare
Medical DeviceDec 21, 2022
STRADIS HEALTHCARE, Surg Pack, Item No.40450SMS, dental recall — FDA Z-0485-2023
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…
Class IIFDA: OngoingStradis Medical, LLC dba Stradis Healthcare
Medical DeviceDec 21, 2022
Zimmer NexGen Option Stemmed Tibial Component Size 7, Item Number 00-5986-057-01 recall — FDA Z-0470-2023
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…
Class IIFDA: OngoingZimmer, Inc.
Medical DeviceDec 21, 2022
STRADIS HEALTHCARE, Basic Implant Pack, Item No.40561BIP, oral surgery tray recall — FDA Z-0488-2023
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…
Class IIFDA: OngoingStradis Medical, LLC dba Stradis Healthcare
Medical DeviceDec 21, 2022
DeRoyal BASIC NEURO PACK, REF 89-7258.10 recall — FDA Z-0590-2023
DeRoyal procedure packs that contain the affected 3M Health Care Steri Drapes which have been recalled.
Class IIFDA: OngoingDeRoyal Industries Inc.
Medical DeviceDec 21, 2022
Stradis Medical, LLC dba Stradis Healthcare Surgical room, Implant Pack, Item No.41111UTI recall — FDA Z-0494-2023
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…
Class IIFDA: OngoingStradis Medical, LLC dba Stradis Healthcare
Medical DeviceDec 21, 2022
Stradis Medical, LLC dba Stradis Healthcare HENRY SCHEIN, PACEMAKER PACK IItem No.570-2793 recall — FDA Z-0519-2023
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…
Class IIFDA: OngoingStradis Medical, LLC dba Stradis Healthcare
Medical DeviceDec 21, 2022
Stradis Medical, LLC dba Stradis Healthcare HENRY SCHEIN, Labiaplasty PackItem No.570-3118 recall — FDA Z-0533-2023
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…
Class IIFDA: OngoingStradis Medical, LLC dba Stradis Healthcare
Medical DeviceDec 21, 2022
STRADIS HEALTHCARE, Phleb, Item No.682-1425 recall — FDA Z-0540-2023
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…
Class IIFDA: OngoingStradis Medical, LLC dba Stradis Healthcare
Medical DeviceDec 21, 2022
Stradis Medical, LLC dba Stradis Healthcare HENRY SCHEIN, Vas Pack, Item No.888-2520 recall — FDA Z-0556-2023
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…
Class IIFDA: OngoingStradis Medical, LLC dba Stradis Healthcare
Medical DeviceDec 21, 2022
DeRoyal PEDI ORTHO PACK, REF 89-5323.20 recall — FDA Z-0565-2023
DeRoyal procedure packs that contain the affected 3M Health Care Steri Drapes which have been recalled.
Class IIFDA: OngoingDeRoyal Industries Inc.
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Recent recall archives
Browse recent months with enough recall history for useful comparison.
October 2026110 records · 3 categoriesSeptember 2026364 records · 4 categoriesAugust 2026302 records · 4 categoriesJuly 2026370 records · 4 categoriesJune 2026376 records · 4 categoriesMay 2026340 records · 4 categoriesApril 2026415 records · 4 categoriesMarch 2026190 records · 4 categoriesFebruary 2026331 records · 4 categoriesJanuary 2026212 records · 4 categoriesDecember 2025389 records · 4 categoriesNovember 2025326 records · 4 categories