DrugApr 16, 2025
Alchemee Proactiv Emergency Blemish Relief (Benzoyl Peroxide 5%), 0.33 oz. (9.45 g) recall — FDA D-0359-2025
Chemical contamination: Presence of benzene
Class IIFDA: OngoingAlchemee, LLC
April 2025 recalls — page 8
These records include useful source details for the selected month.
DrugApr 16, 2025
Haloperidol Decanoate Injection 100mg/mL, 1mL Single-Dose Vial recall — FDA D-0357-2025
Lack of Assurance of Sterility: Media fill with bacterial contamination
Class IIFDA: OngoingSomerset Therapeutics Private Limited
DrugApr 16, 2025
Gabapentin Capsules, USP 300 mg recall — FDA D-0311-2025
Cross Contamination
Class IIIFDA: OngoingSUN PHARMACEUTICAL INDUSTRIES INC
DrugApr 16, 2025
SODIUM CHLORIDE 0.9% Sodium chloride Irrigation USP, Isotonic Solution for Irrigation, 500 recall — FDA D-0353-2025
Presence of Particulate Matter
Class IIFDA: OngoingB. Braun Medical Inc
DrugApr 16, 2025
Alchemee Proactiv Skin Smoothing Exfoliator (Benzoyl Peroxide 2.5%), Packaged as a) 6 fl. recall — FDA D-0360-2025
Chemical contamination: Presence of benzene
Class IIFDA: OngoingAlchemee, LLC
DrugApr 16, 2025
Methocarbamol Injection USP 1,000 mg/10 mL (100 mg/mL), 10 mL Single Dose Vial recall — FDA D-0354-2025
Lack of Assurance of Sterility: Media fill with bacterial contamination
Class IIFDA: OngoingSomerset Therapeutics Private Limited
DrugApr 16, 2025
Venlafaxine Tablets, USP, 75 mg, 100 Tablets recall — FDA D-0310-2025
Presence of Foreign Substance: Product complaint received for the presence of foreign material embedded resembling a metal shaving in one tablet.
Class IIFDA: CompletedZydus Pharmaceuticals (USA) Inc
DrugApr 16, 2025
Gabapentin Capsules, USP 400 mg recall — FDA D-0312-2025
Cross Contamination
Class IIIFDA: OngoingSUN PHARMACEUTICAL INDUSTRIES INC
DrugApr 16, 2025
chlorproMAZINE Hydrochloride Tablets, USP 10 mg recall — FDA D-0361-2025
CGMP deviations: presence of N-Nitroso-Desmethyl Chlorpromazine impurity above the recommended interim limit
Class IIFDA: OngoingZydus Pharmaceuticals (USA) Inc
DrugApr 16, 2025
Sofosbuvir and Velpatasvir, 400 mg/100 mg tablets, 28 tablets: 2x14 blister cards recall — FDA D-0313-2025
Defective Container: blister packs not properly sealed resulting in tablets being loose in the carton.
Class IIFDA: OngoingASEGUA THERAPEUTICS LLC
VehicleApr 11, 2025
Explorer control module software recall — NHTSA campaign 25V239000
Ford Motor Company (Ford) is recalling certain 2025 Explorer vehicles. The powertrain control module (PCM) may reset while driving, which can damage the park system or cause an engine stall.
control module softwareFord Motor Company
VehicleApr 10, 2025
Ram 1500 pressure monitoring and regulating systems recall — NHTSA campaign 25V231000
Chrysler (FCA US, LLC) is recalling certain 2025 Ram 1500 vehicles. A software error may cause an incorrect tire inflation pressure message to display on the instrument panel.
pressure monitoring and regulating systemsChrysler (FCA US, LLC)
Medical DeviceApr 9, 2025
Cordis US Cordis, REF: C09060ML, Smart Control Vascular Stent System ILIAC, 9mm X 60mm 6F recall — FDA Z-1511-2025
product mix-up; Vascular stent labeled as one size but contains a different size.
Class IIFDA: OngoingCordis US Corp
Medical DeviceApr 9, 2025
ID Circuit Flex 220 recall — FDA Z-1494-2025
The potential for cracks forming in the breathing circuit hose.
Class IFDA: OngoingDraeger, Inc.
Medical DeviceApr 9, 2025
Ethicon Endo Surgery PDSII¿VIO¿30IN(75CM)¿USP6-0(M0.7)¿D/A¿C-1 recall — FDA Z-1514-2025
Identified curing issues with the silicone during the needles manufacturing process.
Class IIFDA: OngoingEthicon Endo Surgery, LLC
Medical DeviceApr 9, 2025
Beckman Coulter DxC 500 AU Clinical Chemistry Analyzer, Catalog Numbers/UDI codes: C63519 / recall — FDA Z-1517-2025
Beckman Coulter has determined that device software versions V1.3, V1.4, V1.4.1, V1.4.2, V1.4.3. have a defect due of which, when all constituent tests of a calculated result are rerun,…
Class IIFDA: OngoingBeckman Coulter Inc.
Medical DeviceApr 9, 2025
Stryker Nasopore 4cm Standard 2PK fragmentable nasal dressing, Catalog Number 5400-212-004S recall — FDA Z-1480-2025
There is a potential for blister seals on the product to present a bubble on the seal area of the packaging. This seal acts as a sterile barrier and, in this event, indicates that the…
Class IIFDA: OngoingStryker Corporation
Medical DeviceApr 9, 2025
Ethicon Endo Surgery ETHIBOND EXCEL GRN 36IN(90CM) USP2-0(M3) D/A MH recall — FDA Z-1516-2025
Identified curing issues with the silicone during the needles manufacturing process.
Class IIFDA: OngoingEthicon Endo Surgery, LLC
Medical DeviceApr 9, 2025
Anesthesia Circuit Kit Flex (P)2 recall — FDA Z-1498-2025
The potential for cracks forming in the breathing circuit hose.
Class IFDA: OngoingDraeger, Inc.
Medical DeviceApr 9, 2025
Anesthesia Circuit Kit Flex 2 recall — FDA Z-1496-2025
The potential for cracks forming in the breathing circuit hose.
Class IFDA: OngoingDraeger, Inc.
Medical DeviceApr 9, 2025
Anesthesia Circuit Kit Flex 6 recall — FDA Z-1497-2025
The potential for cracks forming in the breathing circuit hose.
Class IFDA: OngoingDraeger, Inc.
Medical DeviceApr 9, 2025
Stryker Otopore Cylinder Standard outer ear dressings, Catalog Numbers 5400-010-000 and recall — FDA Z-1469-2025
There is a potential for blister seals on the product to present a bubble on the seal area of the packaging. This seal acts as a sterile barrier and, in this event, indicates that the…
Class IIFDA: OngoingStryker Corporation
Medical DeviceApr 9, 2025
GE Healthcare Centricity Universal Viewer (UV), Model Numbers: 1) 2066908-077 recall — FDA Z-1483-2025
There is a potential security vulnerability in Centricity Universal Viewer (UV), Centricity PACS-IW (PACS-IW), Centricity Radiology RA600 (RA600), & Centricity Cardiology CA1000 (CA1000)…
Class IIFDA: OngoingGE Healthcare
Medical DeviceApr 9, 2025
Medtronic Neuromodulation A820 myPTM Software Application associated with Medtronic recall — FDA Z-1506-2025
Product complaints were received describing the A820 myPTM app taking longer than expected for patients to interact with their implantable pump.
Class IIFDA: OngoingMedtronic Neuromodulation
How to use this monthly recall archive
Use this page to compare the recalls reported during the month, then open an individual record for the exact reason, classification, company, remedy or distribution information available from the official source. Monthly counts are descriptive, not a safety rating.