DrugDec 28, 2022
Oxcarbazepine Tablets 600mg recall — FDA D-0085-2023
Presence of foreign substance
Class IIFDA: TerminatedSUN PHARMACEUTICAL INDUSTRIES Inc.
Latest records
Latest recalls — page 640
The newest recall records with useful source details are listed here.
DrugDec 28, 2022
Quinapril Tablets USP, 20 mg (90 pack) recall — FDA D-0089-2023
CGMP Deviations: Detection of N-Nitroso-quinapril impurity above the acceptable daily intake limit.
Class IIFDA: TerminatedLupin Pharmaceuticals Inc.
VehicleDec 22, 2022
Acura TLX bead recall — NHTSA campaign 22V950000
Honda (American Honda Motor Co.) is recalling certain 2022 Acura TLX vehicles. The tires may have sustained cuts and tears during the sorting process, which can result in tire damage.
beadHonda (American Honda Motor Co.)
VehicleDec 22, 2022
Chrysler camera recall — NHTSA campaign 22V947000
Chrysler (FCA US, LLC) is recalling certain 2022 Ram Promaster Chassis Cab and incomplete vehicles equipped with an analog rearview camera. The analog rearview camera is the incorrect type…
cameraChrysler (FCA US, LLC)
Medical DeviceDec 21, 2022
Stradis Medical, LLC dba Stradis Healthcare HENRY SCHEIN, ILR Insertion Tray, Item recall — FDA Z-0534-2023
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 CRANI PACK, REF 89-10242.04 recall — FDA Z-0684-2023
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, BREAST PACK, Item No.570-2397 recall — FDA Z-0509-2023
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, Custom Pack, Item No.41213ATCP, dental recall — FDA Z-0496-2023
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 Industries GEO-MED PODIATRY PACK PGYBK, REF 89-6240.05 recall — FDA Z-0570-2023
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
Leica MICROSYSTEMS Proveo 8, Part Number 10449058, surgical microscope system recall — FDA Z-0475-2023
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…
Class IIFDA: OngoingLeica Microsystems, Inc.
Medical DeviceDec 21, 2022
DeRoyal CATARACT PACK, REF 89-10086.05 recall — FDA Z-0715-2023
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 PACK, REF 89-4051.09 recall — FDA Z-0562-2023
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 BASIC NEURO PACK, REF 89-7258.13 recall — FDA Z-0592-2023
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 CUSTOM NEURO PACK, REF 89-8392.09 recall — FDA Z-0616-2023
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 HEALTHCARE, SAFETY PINS, SMALL 1" Item No.515-001 recall — FDA Z-0499-2023
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 ENDOVENOUS PACK, REF 89-7762.05 recall — FDA Z-0602-2023
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 HEALTHCARE, PROBE COVER W/GEL PACK, Item No.525-071, general surgery tray recall — FDA Z-0501-2023
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 89-7515.14 recall — FDA Z-0598-2023
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
ConMed Foot Controlled Electrosurgical Suction Coagulator, Electrosurgical Suction recall — FDA Z-0474-2023
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…
Class IIFDA: TerminatedConMed Corporation
Medical DeviceDec 21, 2022
Stradis Medical, LLC dba Stradis Healthcare Surgical room, DENTAL SURGICAL PACK, Item recall — FDA Z-0497-2023
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
Siemens Healthcare Diagnostics IMMULITE 2000 Systems 3gAllergy Specific IgE Universal Kit recall — FDA Z-0717-2023
Potential for falsely elevated specific IgE mold allergen reactivity with quality control material and patient samples, may result in false reactive result
Class IIFDA: OngoingSiemens Healthcare Diagnostics, Inc.
Medical DeviceDec 21, 2022
Zimmer NexGen Option Stemmed Tibial Component Size 3, Item Number 00-5986-037-01 recall — FDA Z-0466-2023
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, CUSTOM PK 2, Item No.570-3072 recall — FDA Z-0529-2023
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, Ablation Pack, Item No.682-130 recall — FDA Z-0539-2023
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
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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