DrugMay 15, 2024
Amphotericin B Liposome for Injection, 50mg vials recall — FDA D-0493-2024
Out of specification for assay
Class IIFDA: OngoingSUN PHARMACEUTICAL INDUSTRIES Inc.
Monthly breakdown
2024 recalls by month
Select a month to review the recall records reported during that period.
December 2024325 records · 4 categoriesNovember 2024355 records · 4 categoriesOctober 2024409 records · 4 categoriesSeptember 2024547 records · 4 categoriesAugust 2024327 records · 4 categoriesJuly 2024318 records · 4 categoriesJune 2024286 records · 4 categoriesMay 2024422 records · 4 categoriesApril 2024323 records · 4 categoriesMarch 2024332 records · 4 categoriesFebruary 2024425 records · 4 categoriesJanuary 2024298 records · 4 categories
2024 recalls — page 120
Records are ordered by the best available source date.
DrugMay 15, 2024
Timolol Maleate Ophthalmic Solution, USP, 0.5% recall — FDA D-0488-2024
Defective Container: yellow-colored spike from cap lodged in the nozzle. Firm received several complaints from customers.
Class IIFDA: TerminatedFDC Limited
VehicleMay 15, 2024
BMW front recall — NHTSA campaign 24V345000
BMW of North America, LLC (BMW) is recalling certain 2024 XM, 2025 BMW X5 sDrive40i, X5 xDrive40i, X5 M60i, X5 M, X5 xDrive50e, X6 xDrive40i, X6 M60i, X6 M, X7 xDrive40i, X7 M60i, and…
frontBMW of North America, LLC
VehicleMay 10, 2024
Ford control module (tcm/pcm/tecm) recall — NHTSA campaign 24V330000
Ford Motor Company (Ford) is recalling certain 2022-2024 Maverick, 2020-2022 Escape, and 2021-2022 Lincoln Corsair vehicles. The Hybrid Powertrain Control Module (HPCM) software may cause…
control module (tcm/pcm/tecm)Ford Motor Company
VehicleMay 10, 2024
X5 xDrive40i labels recall — NHTSA campaign 24V327000
BMW of North America, LLC (BMW) is recalling certain 2024-2025 X5 xDrive40i vehicles. The tire information placard may indicate an incorrect tire size and tire pressure. As such, these…
labelsBMW of North America, LLC
VehicleMay 10, 2024
F-150 column recall — NHTSA campaign 24V329000
Ford Motor Company (Ford) is recalling certain 2024 F-150 vehicles. The steering column lower shaft may have been secured to the steering gear assembly with an incorrect fastener, which can…
columnFord Motor Company
Medical DeviceMay 8, 2024
Zimmer ZPLP recall — FDA Z-1714-2024
Thread form issue for the locking holes in that the locking screws may not properly mate with the plate. The improperly mated screw may not be readily recognizable by the user since the…
Class IIFDA: OngoingZimmer, Inc.
Medical DeviceMay 8, 2024
Abbott Aveir Leadless Pacemaker, REF: LSP112V, STERILEEO recall — FDA Z-1695-2024
Their is a potential that electromagnetic interference may cause leadless pacemaker may result in mode change.
Class IIFDA: OngoingAbbott Medical
Medical DeviceMay 8, 2024
Zimmer ZPLP recall — FDA Z-1711-2024
Thread form issue for the locking holes in that the locking screws may not properly mate with the plate. The improperly mated screw may not be readily recognizable by the user since the…
Class IIFDA: OngoingZimmer, Inc.
Medical DeviceMay 8, 2024
Zimmer ZPLP recall — FDA Z-1722-2024
Thread form issue for the locking holes in that the locking screws may not properly mate with the plate. The improperly mated screw may not be readily recognizable by the user since the…
Class IIFDA: OngoingZimmer, Inc.
Medical DeviceMay 8, 2024
Olympus Corporation of the Americas POWERSEAL 5 mm, 37 cm, Curved Jaw Sealer and Divider recall — FDA Z-1700-2024
Upon initial activation of the seal function, the POWERSEAL non-conformance results in an immediate Incomplete Seal Cycle tone with the accompanying message on the generator screen, and no…
Class IIFDA: OngoingOlympus Corporation of the Americas
Medical DeviceMay 8, 2024
Thoratec HeartMate 3, LVAS Implant Kit, REF:106524INT, Sterile EO, RxOnly recall — FDA Z-1693-2024
Potential for a leak path at the seal interface between the left ventricle assist system inflow cannula and the titanium apical cuff.
Class IFDA: OngoingThoratec Corp.
Medical DeviceMay 8, 2024
Olympus Corporation of the Americas POWERSEAL 5 mm, 23 cm, Curved Jaw Sealer and Divider recall — FDA Z-1699-2024
Upon initial activation of the seal function, the POWERSEAL non-conformance results in an immediate Incomplete Seal Cycle tone with the accompanying message on the generator screen, and no…
Class IIFDA: OngoingOlympus Corporation of the Americas
Medical DeviceMay 8, 2024
RAYSEARCH LABORATORIES AB RayStation 9.1.0.933 and 9.2.0.483 recall — FDA Z-1745-2024
Potential for reported SSD to be too high.
Class IIFDA: OngoingRAYSEARCH LABORATORIES AB
Medical DeviceMay 8, 2024
IVOCLAR VIVADENT AG IPS e.max ZirCAD CER/in recall — FDA Z-1704-2024
Defective blocks may show cracks after sintering If cracks are unnoticed, restorations may fracture in the patient's mouth and require restoration
Class IIFDA: OngoingIVOCLAR VIVADENT AG
Medical DeviceMay 8, 2024
Covidien Sofsilk Braided Silk sutures, Product Number S-2782K recall — FDA Z-1697-2024
One lot of product was exposed to more than the approved number of Ethylene Oxide (EO) sterilization cycles. This may decrease the tensile strength of the sutures over time, which could…
Class IIFDA: OngoingCovidien, LP
Medical DeviceMay 8, 2024
Zimmer ZPLP Distal Lateral Fibular Plate, Right, 10 Holes, 158 MM, Nonsterile- Indicated for recall — FDA Z-1725-2024
Thread form issue for the locking holes in that the locking screws may not properly mate with the plate. The improperly mated screw may not be readily recognizable by the user since the…
Class IIFDA: OngoingZimmer, Inc.
Medical DeviceMay 8, 2024
Zimmer ZPLP Distal Lateral Fibular Plate, Left, 8 Holes, 132 MM, Nonsterile-Indicated for recall — FDA Z-1728-2024
Thread form issue for the locking holes in that the locking screws may not properly mate with the plate. The improperly mated screw may not be readily recognizable by the user since the…
Class IIFDA: OngoingZimmer, Inc.
Medical DeviceMay 8, 2024
IVOCLAR VIVADENT AG IPS e.max ZirCAD CER/in recall — FDA Z-1707-2024
Defective blocks may show cracks after sintering If cracks are unnoticed, restorations may fracture in the patient's mouth and require restoration
Class IIFDA: OngoingIVOCLAR VIVADENT AG
Medical DeviceMay 8, 2024
Zimmer ZPLP Distal Lateral Fibular Plate, Left, 4 Holes, 80 MM, Sterile- Indicated for recall — FDA Z-1715-2024
Thread form issue for the locking holes in that the locking screws may not properly mate with the plate. The improperly mated screw may not be readily recognizable by the user since the…
Class IIFDA: OngoingZimmer, Inc.
Medical DeviceMay 8, 2024
RAYSEARCH LABORATORIES AB RayStation 12.0.0.932, 12.1.0.1221, 12.0.3.68, 12.0.4.12 recall — FDA Z-1749-2024
Potential for reported SSD to be too high.
Class IIFDA: OngoingRAYSEARCH LABORATORIES AB
Medical DeviceMay 8, 2024
Zimmer ZPLP Distal Lateral Fibular Plate, Left, 10 Holes, 158 MM, Nonsterile-Indicated for recall — FDA Z-1729-2024
Thread form issue for the locking holes in that the locking screws may not properly mate with the plate. The improperly mated screw may not be readily recognizable by the user since the…
Class IIFDA: OngoingZimmer, Inc.
Medical DeviceMay 8, 2024
IVOCLAR VIVADENT AG IPS e.max ZirCAD CER/in recall — FDA Z-1705-2024
Defective blocks may show cracks after sintering If cracks are unnoticed, restorations may fracture in the patient's mouth and require restoration
Class IIFDA: OngoingIVOCLAR VIVADENT AG
Medical DeviceMay 8, 2024
ADVANCED RESEARCH MEDICAL Lumbar Interbody Fusion System (OLLIF), Flexible Curette Loop recall — FDA Z-1698-2024
Potential shearing of the disposable blade may occur and be contained within the of Flexible Curette Shaft Assembly during surgery.
Class IIFDA: CompletedAdvanced Research Medical, LLC
About the 2024 recall archive
This archive groups records by their reported or recall date. It does not imply that every recall was initiated, announced and resolved during the same calendar year. Open the individual record for the exact dates and source details supplied by FDA or NHTSA.