Latest U.S. Recalls — FDA & NHTSA Records

Latest records

Latest recalls — page 241

The newest recall records with useful source details are listed here.

DrugSep 6, 2023

Central Admixture Pharmacy Services EPINEPHrine, 2 mg added to dextrose 5% 250mL recall — FDA D-1129-2023

Lack of Assurance of Sterility:Lack of validation data for sanitization cycles

Class IIFDA: TerminatedCentral Admixture Pharmacy Services, Inc.

VehicleSep 6, 2023

Jetta instrument cluster/panel recall — NHTSA campaign 23V619000

Volkswagen Group of America, Inc. (Volkswagen) is recalling certain 2019 Jetta vehicles. The instrument cluster may not provide an audible warning to let the driver know that the key is…

instrument cluster/panelVolkswagen Group of America, Inc.

VehicleAug 31, 2023

Kia camera recall — NHTSA campaign 23V610000

Kia America, Inc. (Kia) is recalling certain 2022-2023 Sorento, Sorento Hybrid, and Sorento Plug-in Hybrid (PHEV) vehicles. The mounting clips for the rearview camera may break, which can…

cameraKia America, Inc.

DrugAug 30, 2023

Ecometics YAGER'S LINIMENT recall — FDA D-1097-2023

CGMP Deviations: Products not manufactured under current good manufacturing practices.

Class IIFDA: CompletedEcometics, Inc.

DrugAug 30, 2023

Parker Laboratories Protex Foaming Hand Sanitizer recall — FDA D-1089-2023

CGMP Deviations

Class IIFDA: TerminatedParker Laboratories, Inc.

DrugAug 30, 2023

Parker Laboratories Helix CBD Clinical Cream (Menthol 7.4%) recall — FDA D-1093-2023

CGMP Deviations

Class IIFDA: TerminatedParker Laboratories, Inc.

DrugAug 30, 2023

Trandolapril and Verapamil Hydrochloride Extended-Release Tablets 2 mg / 180 mg, 100-count recall — FDA D-1095-2023

Subpotent: Out of Specification for Assay Test at the 3-month time point.

Class IIIFDA: OngoingGlenmark Pharmaceuticals Inc., USA

DrugAug 30, 2023

Ecometics Unguentine Ointment recall — FDA D-1099-2023

CGMP Deviations: Products not manufactured under current good manufacturing practices.

Class IIFDA: CompletedEcometics, Inc.

DrugAug 30, 2023

Bendamustine HCl Injection, 100mg/4mL (25mg/mL), One 4 mL Multiple-Dose Vial recall — FDA D-1103-2023

Labeling: Missing Label; customer complaint received that labels were partially or completely peeled off injection vial.

Class IIIFDA: CompletedBaxter Healthcare Corporation

DrugAug 30, 2023

Inmar Supply Chain Solutions All Over-The-Counter (OTC) drug products warehoused, salvaged recall — FDA D-1104-2023

CGMP Deviations: Potential exposure to rodents and rodent activity in the distribution center. Also, due to unusually hot weather, FDA Recalled Products may have been subjected to…

Class IIFDA: OngoingInmar Supply Chain Solutions, LLC

DrugAug 30, 2023

Parker Laboratories Helix CBD Therapy Cream (Menthol 7.4%) recall — FDA D-1092-2023

CGMP Deviations

Class IIFDA: TerminatedParker Laboratories, Inc.

DrugAug 30, 2023

Ecometics Blis-To-Sol Liquid (Tolnaftate), 1% recall — FDA D-1096-2023

CGMP Deviations: Products not manufactured under current good manufacturing practices.

Class IIFDA: CompletedEcometics, Inc.

DrugAug 30, 2023

Parker Laboratories Helix Tri-Active Therapy Cream recall — FDA D-1091-2023

CGMP Deviations

Class IIFDA: TerminatedParker Laboratories, Inc.

DrugAug 30, 2023

Ecometics ALCOLADO RELAMPAGO (Menthol and Camphor), 1% and 1.5% respectively recall — FDA D-1098-2023

CGMP Deviations: Products not manufactured under current good manufacturing practices.

Class IIFDA: CompletedEcometics, Inc.

DrugAug 30, 2023

Ecometics Lugol's recall — FDA D-1102-2023

CGMP Deviations: Products not manufactured under current good manufacturing practices.

Class IIFDA: CompletedEcometics, Inc.

DrugAug 30, 2023

Parker Laboratories Helix Pain Relieving Cream (Menthol 7.4%) recall — FDA D-1090-2023

CGMP Deviations

Class IIFDA: TerminatedParker Laboratories, Inc.

VehicleAug 30, 2023

Volkswagen Group of switch recall — NHTSA campaign 23V604000

Volkswagen Group of America, Inc. (Volkswagen) is recalling certain 2019 Golf, Golf Alltrack, Golf Sportwagen, 2019-2020 Golf GTI, and Jetta vehicles equipped with a conventional ignition…

switchVolkswagen Group of America, Inc.

VehicleAug 25, 2023

Volkswagen Group of fluid recall — NHTSA campaign 23V601000

Volkswagen Group of America, Inc. (Audi) is recalling certain 2021 Audi S7, S6 Sedan, RS7, RS6 Avant, A6 Allroad, 2019-2021 A7, and A6 Sedan vehicles. An incorrectly labeled brake fluid cap…

fluidVolkswagen Group of America, Inc.

VehicleAug 25, 2023

Palisade front passenger recall — NHTSA campaign 23V599000

Hyundai Motor America (Hyundai) is recalling certain 2024 Palisade vehicles equipped with dark premium suede seats. The Occupant Detection System (ODS) may fail to detect an occupant and…

front passengerHyundai Motor America

VehicleAug 25, 2023

Ford camera recall — NHTSA campaign 23V598000

Ford Motor Company (Ford) is recalling certain 2020-2023 Lincoln Aviator, 2018-2021 Lincoln Navigator, 2022-2023 Ford Transit, and 2021 Ford Bronco vehicles. The rearview camera, or…

cameraFord Motor Company

VehicleAug 25, 2023

Explorer turbo/supercharger recall — NHTSA campaign 23V597000

Ford Motor Company (Ford) is recalling certain 2023 Explorer vehicles equipped with 2.3L GTDI engines. The turbocharger oil supply line may be damaged, which can result in an oil leak…

turbo/superchargerFord Motor Company

DrugAug 23, 2023

Advanced Accelerator Applications USA PLUVICTO 1,000MBq/mL (27 mCi/mL), lutetium Lu 177 recall — FDA D-1085-2023

Labeling: Incorrect or Missing Lot and/or Exp Date: vials were labeled with the incorrect lot number and expiration date

Class IIIFDA: TerminatedAdvanced Accelerator Applications USA, Inc.

DrugAug 23, 2023

Colgate Palmolive Company hello wild strawberry fluoride toothpaste, sodium fluoride 0.24% recall — FDA D-1084-2023

Labeling: Label Mix-Up: Some hello wild strawberry fluoride toothpaste, packaged in cartons labeled as hello wild strawberry fluoride toothpaste were incorrectly filled in tubes labeled as…

Class IIFDA: TerminatedColgate Palmolive Company

DrugAug 16, 2023

SODIUM CHLORIDE 0.9% Sodium Chloride Injection USP, 1000 mL Excel Plus Container recall — FDA D-1083-2023

Labeling: Not Elsewhere Classified - the description, warnings, storage information and instructions for use are either missing or partially printed.

Class IIIFDA: TerminatedB. Braun Medical Inc.

Browse by month

Recent recall archives

Browse recent months with enough recall history for useful comparison.

Full archive →