DrugJan 31, 2024
Fosaprepitant for Injection 150 mg per vial, Sterile lyophilized powder for Intravenous use recall — FDA D-0262-2024
Lack of Sterility Assurance: Aseptic process simulation failure.
Class IIFDA: TerminatedBE PHARMACEUTICALS AG
Latest records
Latest recalls — page 230
The newest recall records with useful source details are listed here.
DrugJan 31, 2024
Fexofenadine Hydrochloride Tablets, USP 180mg, Antihistamine, Allergy, 24 hour, a) 30 recall — FDA D-0273-2024
CGMP Deviations: Microbial contamination was reported in stagnant water in the duct of the manufacturing equipment.
Class IIFDA: CompletedSUN PHARMACEUTICAL INDUSTRIES Inc.
DrugJan 31, 2024
Benzonatate Capsules, USP, 100 mg, 100 Capsules recall — FDA D-0257-2024
Superpotent drug: Assay results were slightly above specification at the time zero point.
Class IIIFDA: OngoingAmerisource Health Services LLC
DrugJan 31, 2024
Zolpidem Tartrate Extended-Release Tablets, USP 6.25 mg recall — FDA D-0271-2024
CGMP Deviations: Microbial contamination was reported in stagnant water in the duct of the manufacturing equipment.
Class IIFDA: CompletedSUN PHARMACEUTICAL INDUSTRIES Inc.
DrugJan 31, 2024
Febuxostat Tablets 40mg recall — FDA D-0264-2024
CGMP Deviations: Microbial contamination was reported in stagnant water in the duct of the manufacturing equipment.
Class IIFDA: CompletedSUN PHARMACEUTICAL INDUSTRIES Inc.
DrugJan 31, 2024
Febuxostat Tablets 80 mg recall — FDA D-0265-2024
CGMP Deviations: Microbial contamination was reported in stagnant water in the duct of the manufacturing equipment.
Class IIFDA: CompletedSUN PHARMACEUTICAL INDUSTRIES Inc.
DrugJan 31, 2024
Niacin Extended-Release Tablets, USP 1000mg recall — FDA D-0269-2024
CGMP Deviations: Microbial contamination was reported in stagnant water in the duct of the manufacturing equipment.
Class IIFDA: CompletedSUN PHARMACEUTICAL INDUSTRIES Inc.
DrugJan 31, 2024
Niacin Extended-Release Tablets, USP 500mg recall — FDA D-0270-2024
CGMP Deviations: Microbial contamination was reported in stagnant water in the duct of the manufacturing equipment.
Class IIFDA: CompletedSUN PHARMACEUTICAL INDUSTRIES Inc.
DrugJan 31, 2024
Lurasidone Hydrochloride Tablets 120mg recall — FDA D-0267-2024
CGMP Deviations: Microbial contamination was reported in stagnant water in the duct of the manufacturing equipment.
Class IIFDA: CompletedSUN PHARMACEUTICAL INDUSTRIES Inc.
DrugJan 31, 2024
Cinacalcet Tablets 60mg recall — FDA D-0263-2024
CGMP Deviations: Microbial contamination was reported in stagnant water in the duct of the manufacturing equipment.
Class IIFDA: CompletedSUN PHARMACEUTICAL INDUSTRIES Inc.
DrugJan 31, 2024
Mesalamine Delayed-Release Tablets, USP 1.2 g per tablet recall — FDA D-0268-2024
CGMP Deviations: Microbial contamination was reported in stagnant water in the duct of the manufacturing equipment.
Class IIFDA: CompletedSUN PHARMACEUTICAL INDUSTRIES Inc.
DrugJan 31, 2024
Zolpidem Tartrate Extended-Release Tablets, USP 12.5mg recall — FDA D-0272-2024
CGMP Deviations: Microbial contamination was reported in stagnant water in the duct of the manufacturing equipment.
Class IIFDA: CompletedSUN PHARMACEUTICAL INDUSTRIES Inc.
DrugJan 31, 2024
Lurasidone Hydrochloride Tablets 60mg recall — FDA D-0266-2024
CGMP Deviations: Microbial contamination was reported in stagnant water in the duct of the manufacturing equipment.
Class IIFDA: CompletedSUN PHARMACEUTICAL INDUSTRIES Inc.
VehicleJan 30, 2024
Tesla instrument cluster/panel recall — NHTSA campaign 24V051000
Tesla, Inc. (Tesla) is recalling certain 2012-2023 Model S, 2016-2024 Model X, 2017-2023 Model 3, 2019-2024 Model Y, and 2024 Cybertruck vehicles. An incorrect font size is displayed on the…
instrument cluster/panelTesla, Inc.
DrugJan 24, 2024
The Procter & Gamble Company Secret, Dry Spray recall — FDA D-0245-2024
CGMP Deviation; manufactured at the same facility where other lots were found to be contaminated with benzene
Class IIFDA: TerminatedThe Procter & Gamble Company
DrugJan 24, 2024
The Procter & Gamble Company Secret, Dry Spray recall — FDA D-0255-2024
CGMP Deviation; manufactured at the same facility where other lots were found to be contaminated with benzene
Class IIFDA: TerminatedThe Procter & Gamble Company
DrugJan 24, 2024
The Procter & Gamble Company Secret, Dry Spray recall — FDA D-0243-2024
Chemical contamination: presence of benzene
Class IFDA: TerminatedThe Procter & Gamble Company
DrugJan 24, 2024
The Procter & Gamble Company Old Spice, SWEAT DEFENSE PURE SPORT PLUS, Dry Spray recall — FDA D-0240-2024
Chemical contamination: presence of benzene
Class IFDA: TerminatedThe Procter & Gamble Company
DrugJan 24, 2024
Atropine Sulfate Injection, USP 1 mg/10 mL (0.1 mg/mL), Lifeshield, Glass ABBOJECT Unit of recall — FDA D-0235-2024
Presence of Particulate Matter; identified as glass
Class IFDA: OngoingPfizer Inc.
DrugJan 24, 2024
The Procter & Gamble Company Old Spice, SWEAT DEFENSE ULTIMATE CAPTAIN, Aluminum recall — FDA D-0241-2024
Chemical contamination: presence of benzene
Class IFDA: TerminatedThe Procter & Gamble Company
DrugJan 24, 2024
The Procter & Gamble Company Old Spice, PURE SPORT recall — FDA D-0250-2024
CGMP Deviation; manufactured at the same facility where other lots were found to be contaminated with benzene
Class IIFDA: TerminatedThe Procter & Gamble Company
DrugJan 24, 2024
AMERICAINE recall — FDA D-0236-2024
Chemical Contamination: presence of benzene
Class IFDA: CompletedInsight Pharmaceuticals LLC, a Prestige Consumer…
DrugJan 24, 2024
SODIUM BICARBONATE 8.4 % Sodium Bicarbonate Injection, USP 50 mEq/50 mL (1 mEq/mL) recall — FDA D-0234-2024
Presence of Particulate Matter; identified as glass
Class IFDA: OngoingPfizer Inc.
DrugJan 24, 2024
The Procter & Gamble Company Secret, Dry Spray, Aluminum chlorohydrate 23.5% Antiperspirant recall — FDA D-0254-2024
CGMP Deviation; manufactured at the same facility where other lots were found to be contaminated with benzene
Class IIFDA: TerminatedThe Procter & Gamble Company
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