DrugJan 18, 2023
Northern VA Compounders PLLC TriMix Injection recall — FDA D-0118-2023
Lack of Assurance of Sterility
Class IIFDA: TerminatedNorthern VA Compounders PLLC
Latest records
Latest recalls — page 326
The newest recall records with useful source details are listed here.
DrugJan 18, 2023
Northern VA Compounders PLLC TriMix Injection recall — FDA D-0115-2023
Lack of Assurance of Sterility
Class IIFDA: TerminatedNorthern VA Compounders PLLC
DrugJan 18, 2023
Northern VA Compounders PLLC QuadMix Plus recall — FDA D-0103-2023
Lack of Assurance of Sterility
Class IIFDA: TerminatedNorthern VA Compounders PLLC
DrugJan 11, 2023
Acyclovir Sodium Injection 1,000 mg per 20 mL* (50 mg/mL) recall — FDA D-0095-2023
Presence of Particulate Matter: Customer complaint of dark particles found inside the vial
Class IIFDA: OngoingEugia US LLC
DrugJan 11, 2023
Heparin Sodium 2,000, USP Units, per 1,000 mL (2 USP Units/mL) in 0.9% Sodium Chloride recall — FDA D-0097-2023
Lack of assurance of sterility: Bags have the potential to leak.
Class IIFDA: CompletedPfizer Inc.
VehicleJan 5, 2023
Volvo Car USA steering recall — NHTSA campaign 23V001000
Volvo Car USA, LLC (Volvo Car) is recalling certain 2019-2022 V60CC, XC60, and XC90 vehicles. During steering gear assembly, double screws may have been assembled on top of each other,…
steeringVolvo Car USA, LLC
DrugJan 4, 2023
Apotex Timolol Maleate Ophthalmic Solution, USP 0.5%, 2.5 mL recall — FDA D-0093-2023
Failed Stability Specifications: Out of specification for weight loss at the 18-month stability timepoint and projected weight loss of 21.1% at shelf life.
Class IIIFDA: TerminatedApotex Corp.
DrugJan 4, 2023
Ganciclovir for Injection, USP, 500mg per vial recall — FDA D-0090-2023
Labeling: Label mix-up - one vial was mislabeled as Cladribine Injection 10mg/mL inside a 10-count carton of Ganciclovir 500 mg.
Class IIFDA: TerminatedHikma Pharmaceuticals USA Inc.
DrugJan 4, 2023
NCH Life Sciences Alcohol Antiseptic 80% Topical Solution Hand Sanitizer, Non-Sterile recall — FDA D-0092-2023
CGMP Deviations: Impurities of acetal and acetaldehyde were discovered in the product in excess of allowed limits.
Class IIFDA: CompletedNCH Life Sciences LLC
DrugDec 28, 2022
Quinapril Tablets USP, 40 mg (90 pack) recall — FDA D-0088-2023
CGMP Deviations: Detection of N-Nitroso-quinapril impurity above the acceptable daily intake limit.
Class IIFDA: TerminatedLupin Pharmaceuticals Inc.
DrugDec 28, 2022
Oxcarbazepine Tablets 600mg recall — FDA D-0085-2023
Presence of foreign substance
Class IIFDA: TerminatedSUN PHARMACEUTICAL INDUSTRIES Inc.
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)
DrugDec 21, 2022
BayCare Integrated Service Center, LLC /dba Iohexol (300 mg Iodine/mL), 2.4 g Iodine/8 ml recall — FDA D-0086-2023
Labeling: Label Error on Declared Strength: syringes mislabeled as 300 mg iodine/mL contained product 350 mg iodine/mL
Class IFDA: TerminatedBayCare Integrated Service Center, LLC /dba BayCare…
DrugDec 21, 2022
SODIUM BICARBONATE 8.4% Sodium Bicarbonate Injection, USP 50 mEq/50 mL (1 mEq/mL) 50 mL recall — FDA D-0079-2023
Defective Container: Complaints received of vial breakage and glass flying when pressurized while preparing the product for administration.
Class IFDA: TerminatedExela Pharma Sciences LLC
DrugDec 21, 2022
Exela Pharma Sciences 8.4% Sodium Bicarbonate Injection, USP 50 mEq/50 mL (1 mEq/mL) 50 mL recall — FDA D-0080-2023
Defective Container: Complaints received of vial breakage and glass flying when pressurized while preparing the product for administration.
Class IFDA: TerminatedExela Pharma Sciences LLC
DrugDec 21, 2022
Lacosamide Oral Solution, USP, CV, 10mg/mL recall — FDA D-0094-2023
Failed Excipient Specifications: out of specification result observed for p-Hydroxybenzoic Acid content
Class IIIFDA: TerminatedCamber Pharmaceuticals, Inc.
VehicleDec 19, 2022
BMW critical fasteners recall — NHTSA campaign 22V942000
BMW of North America, LLC (BMW) is recalling certain 2023 X5 sDrive40i, X5 M50i and X5 xDrive 45e vehicles. One of the four bolts that connects the backrest to the driver's seat frame may…
critical fastenersBMW of North America, LLC
VehicleDec 15, 2022
General Motors front passenger recall — NHTSA campaign 22V929000
General Motors, LLC (GM) is recalling certain 2023 Chevrolet Equinox and GMC Terrain vehicles equipped with ventilated front passenger seats. The Occupant Classification System may not…
front passengerGeneral Motors, LLC
DrugDec 14, 2022
RemedyRepack Desmopressin Acetate Tablet, 0.2 mg, 100-count box recall — FDA D-0077-2023
Subpotent Drug: repackaged product was recalled by the manufacturer for subpotency.
Class IIFDA: TerminatedRemedyRepack Inc.
DrugDec 14, 2022
SODIUM CHLORIDE 0.9% Sodium Chloride Injection, USP, Each 100 mL contains: SODIUM CHLORIDE recall — FDA D-0075-2023
Lack of Assurance of Sterility: Leakage of 0.9% Sodium Chloride for Injection, 1L, 12pk Saline Solution.
Class IIFDA: OngoingFresenius Medical Care Holdings, Inc.
VehicleDec 14, 2022
Bronco side impact recall — NHTSA campaign 22V928000
Ford Motor Company (Ford) is recalling certain 2021-2022 Bronco vehicles. The right or left side impact sensors may not be properly secured to the vehicle.
side impactFord Motor Company
VehicleDec 14, 2022
Chevrolet Malibu frame and members recall — NHTSA campaign 22V923000
General Motors, LLC (GM) is recalling certain 2022-2023 Chevrolet Malibu vehicles. The front impact bar, a structural portion of the vehicle frame, may not be properly welded to the front…
frame and membersGeneral Motors, LLC
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