DrugAug 30, 2023
Parker Laboratories Protex Foaming Hand Sanitizer recall — FDA D-1089-2023
CGMP Deviations
Class IIFDA: TerminatedParker Laboratories, Inc.
Monthly breakdown
2023 recalls by month
Select a month to review the recall records reported during that period.
December 2023295 records · 4 categoriesNovember 2023387 records · 4 categoriesOctober 2023214 records · 4 categoriesSeptember 2023253 records · 4 categoriesAugust 2023478 records · 4 categoriesJuly 2023263 records · 4 categoriesJune 2023339 records · 4 categoriesMay 2023410 records · 4 categoriesApril 2023189 records · 4 categoriesMarch 2023788 records · 4 categoriesFebruary 2023253 records · 4 categoriesJanuary 2023205 records · 4 categories
2023 recalls — page 50
Records are ordered by the best available source date.
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
Medical DeviceAug 23, 2023
Carefusion 2200 Snowden-Pencer MIS DIAMOND-TOUCH DISSECTOR DIAMOND JAW 5MM, 45CM, RATCHETED recall — FDA Z-2429-2023
Specific lots of the product have the potential to exhibit cracking or breaking of the rotation knob due to the incorrect use of an adhesive in the manufacturing process.
Class IIFDA: OngoingCarefusion 2200 Inc.
Medical DeviceAug 23, 2023
Carefusion 2200 Snowden-Pencer MIS DIAMOND-TOUCH ATRAUMATIC GRASPER DIAMOND JAW 5MM, 45CM recall — FDA Z-2426-2023
Specific lots of the product have the potential to exhibit cracking or breaking of the rotation knob due to the incorrect use of an adhesive in the manufacturing process.
Class IIFDA: OngoingCarefusion 2200 Inc.
Medical DeviceAug 23, 2023
Covidien MAHURKAR 12 Fr High Pressure Triple Lumen Acute Dialysis Catheter, 20 cm, Curved recall — FDA Z-2389-2023
Catheter center lumen was found to have an occlusion in the tip of the catheter; the source of the occlusion an excessive MDX, a silicone-based lubricant which coats the catheter tip. An…
Class IFDA: OngoingCovidien LP
Medical DeviceAug 23, 2023
Covidien MAHURKAR 12 Fr High Pressure Triple Lumen Acute Dialysis Catheter, 24 cm, Straight recall — FDA Z-2381-2023
Catheter center lumen was found to have an occlusion in the tip of the catheter; the source of the occlusion an excessive MDX, a silicone-based lubricant which coats the catheter tip. An…
Class IFDA: OngoingCovidien LP
Medical DeviceAug 23, 2023
Covidien MAHURKAR 12 Fr High Pressure Triple Lumen Acute Dialysis Catheter, 16 cm, Curved recall — FDA Z-2387-2023
Catheter center lumen was found to have an occlusion in the tip of the catheter; the source of the occlusion an excessive MDX, a silicone-based lubricant which coats the catheter tip. An…
Class IFDA: OngoingCovidien LP
Medical DeviceAug 23, 2023
Covidien MAHURKAR 12 Fr High Pressure Triple Lumen Acute Dialysis Catheter, 13 cm, Curved recall — FDA Z-2367-2023
Catheter center lumen was found to have an occlusion in the tip of the catheter; the source of the occlusion an excessive MDX, a silicone-based lubricant which coats the catheter tip. An…
Class IFDA: OngoingCovidien LP
Medical DeviceAug 23, 2023
Covidien MAHURKAR 12 Fr High Pressure Triple Lumen Acute Dialysis Catheter, 24 cm, Curved recall — FDA Z-2375-2023
Catheter center lumen was found to have an occlusion in the tip of the catheter; the source of the occlusion an excessive MDX, a silicone-based lubricant which coats the catheter tip. An…
Class IFDA: OngoingCovidien LP
About the 2023 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.