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Consumer Product Recalls
127,277 recalls from the U.S. Consumer Product Safety Commission, newest first.
July 23, 2025DrugsFDA
A.P. Deauville, LLC recalls Power Stick for her PH Balanced Roll-On Antiperspirant Deodorant with Powder Fresh Scent, 1.8 oz./53 mL, A.P Deauville,
Hazard: CGMP Deviations
July 23, 2025DrugsFDA
Ascend Laboratories, LLC recalls Rizatriptan Benzoate Tablets, USP, 10 mg, 18 (3x6) Unit Dose Tablets, Rx Only, Manufactured by: Alkem Laboratories Ltd.,
Hazard: CGMP Deviations: detection of N-nitroso-dimethyl-rizatriptan impurity, above the FDA recommended acceptable intake limit.
July 23, 2025DrugsFDA
Ascend Laboratories, LLC recalls Rizatriptan Benzoate Tablets, USP, 5 mg, 18 (3x6) Unit Dose Tablets, Rx Only, Manufactured by: Alkem Laboratories Ltd.,
Hazard: CGMP Deviations: detection of N-nitroso-dimethyl-rizatriptan impurity, above the FDA recommended acceptable intake limit.
July 23, 2025DrugsFDA
Lupin Pharmaceuticals Inc. recalls Lisinopril and Hydrochlorothiazide Tablets USP 20mg/12.5mg, 100-count bottles, Rx only, Mfg for: Lupin Pharmaceuticals,
Hazard: Product Mix Up: This product is being recalled because of a complaint received that a sealed bottle of lisinopril and hydrochlorothiazide tablets 20mg/12.5 mg had a foreign tablet identified as atazanavir and ritonavir tablet 300mg/100mg.
July 23, 2025DrugsFDA
Central Admixture Pharmacy Services, Inc (CAPS) Los Angeles recalls PERIPHERAL PARENTERAL NUTRITION, Compounded Sterile Preparation, Refrigerated Injection, Rx Only, Single Dose Injection,
Hazard: Lack of Processing Controls; prescriptions were compounded in an ISO-5 area where it was identified that a daily cleaning step was not sufficiently documented.
July 23, 2025DrugsFDA
Dr. Reddy's Laboratories, Inc. recalls Omeprazole Delayed-release Capsules, USP, 20mg, 1000-count bottle, Rx Only, Manufactured by: Dr. Reddy's Laboratories Li
Hazard: Presence of foreign tablets/capsules: presence of foreign Divalproex Sodium Extended-Release 250mg tablet in a bottle of omeprazole capsules.
July 23, 2025DrugsFDA
ACCORD HEALTHCARE, INC. recalls Levothyroxine Sodium Tablets, USP, 175 mcg (0.175 mg), 1000-count bottle, Rx Only, Manufactured for: Accord Healthcare,
Hazard: Subpotent Drug: Assay below the approved specification
July 23, 2025DrugsFDA
ACCORD HEALTHCARE, INC. recalls Levothyroxine Sodium Tablets, USP, 150 mcg (0.15 mg), 1000-count bottle, Rx Only, Manufactured for: Accord Healthcare, I
Hazard: Subpotent Drug: Assay below the approved specification
July 23, 2025DrugsFDA
ACCORD HEALTHCARE, INC. recalls Levothyroxine Sodium Tablets, USP, 112 mcg (0.112 mg), 1000-count bottle, Rx Only, Manufactured for: Accord Healthcare,
Hazard: Subpotent Drug: Assay below the approved specification
July 23, 2025DrugsFDA
ACCORD HEALTHCARE, INC. recalls Levothyroxine Sodium Tablets, USP, 100 mcg (0.1 mg), 1000-count bottle, Rx Only, Manufactured for: Accord Healthcare, In
Hazard: Subpotent Drug: Assay below the approved specification
July 23, 2025DrugsFDA
ACCORD HEALTHCARE, INC. recalls Levothyroxine Sodium Tablets, USP, 50 mcg (0.05 mg), 90-count bottle, Rx Only, Manufactured for: Accord Healthcare, Inc.
Hazard: Subpotent Drug: Assay below the approved specification
July 23, 2025DrugsFDA
ACCORD HEALTHCARE, INC. recalls Levothyroxine Sodium Tablets, USP, 25 mcg (0.025 mg), 1000-count bottle, Rx Only, Manufactured for: Accord Healthcare, I
Hazard: Subpotent Drug: Assay below the approved specification
July 23, 2025DrugsFDA
ACCORD HEALTHCARE, INC. recalls Levothyroxine Sodium Tablets, USP, 25 mcg (0.025 mg), 90-count bottle, Rx Only, Manufactured for: Accord Healthcare, Inc
Hazard: Subpotent Drug: Assay below the approved specification
July 23, 2025DrugsFDA
Qualgen, LLC recalls Testosterone 200 mg Pellet packaged in 1mL amber vials, Rx only, Compounded product. Qualgen 14844 Bristol Park Blvd Edm
Hazard: Labeling: Incorrect or Missing Lot and/or Exp. Date: A printing issue resulted in incorrect lot numbers on the label.
July 23, 2025DrugsFDA
SUN PHARMACEUTICAL INDUSTRIES INC recalls Lisdexamfetamine Dimesylate Capsules, 60 mg, CII, 100-count bottles, Rx only, Manufactured by: OHM Laboratories, New Bru
Hazard: Failed Dissolution Specifications: An out of specification results observed in dissolution test during analysis at 9 month long term stability station (25¿C, 60%RH).
July 23, 2025VehiclesNHTSA
Hyundai 2025 Electrical System recall
Hazard: An electrical short in the high voltage battery system increases the risk of a fire.
July 23, 2025VehiclesNHTSA
Tiffin 2023–2026 Electrical System recall
Hazard: Improper programming can cause the engine to stall, increasing the risk of a crash.
July 23, 2025VehiclesNHTSA
Ferrari 2023–2025 Structure recall
Hazard: A loss of braking ability increases the risk of a crash.
July 23, 2025VehiclesNHTSA
BMW 2022–2025 Electrical System recall
Hazard: A loss of drive power increases the risk of a crash.
July 22, 2025VehiclesNHTSA
Winnebago 2024–2026 Air Bags recall
Hazard: Damaged wires can prevent air bags from deploying in a crash, increasing the risk of injury.
July 22, 2025VehiclesNHTSA
Lamborghini 2024–2025 Structure recall
Hazard: Door spring failure can cause the doors to close unexpectedly, increasing the risk of injury.
July 22, 2025VehiclesNHTSA
Nova BUS 2020–2023 Steering recall
Hazard: A steering wheel that turns unintentionally increases the risk of a crash or injury.
July 21, 2025VehiclesNHTSA
Rosenbauer 2019–2024 Electrical System recall
Hazard: An inaccurate odometer reading can unintentionally delay critical safety-related maintenance, potentially impairing the safe operation of the vehicle and increasing the risk of a crash.
July 21, 2025Sports & RecreationCPSC
Bestway, Intex, and Polygroup Recall Certain Above-Ground Pools 48 Inches and Taller Due to Drowning Hazard; Nine Deaths Reported; Five Million Pools Sold Since 2002
Hazard: The compression strap that surrounds the outside of the pool legs may create a foothold, allowing a child access to the pool, posing a drowning risk.
July 17, 2025VehiclesNHTSA
Genesis 2023–2025 Electrical System recall
Hazard: An instrument panel display that fails to show critical safety information, such as the speedometer or warning lights, increases the risk of a crash.
July 17, 2025VehiclesNHTSA
Grand Design 2025–2026 Equipment recall
Hazard: Door latch failure may prevent occupants from exiting the vehicle in an emergency, increasing the risk of injury.
July 17, 2025VehiclesNHTSA
Jeep 2023–2024 Seats recall
Hazard: Head restraints that do not lock can result in an increased risk of injury to seat occupants during a crash.
July 17, 2025VehiclesNHTSA
Chrysler 2024–2025 Equipment recall
Hazard: A rearview image that does not display reduces the driver's view of what is behind the vehicle, increasing the risk of a crash.
July 17, 2025TiresNHTSA
Michelin Tires recall
Hazard: Tires that are missing a DOT symbol may be used in inappropriate applications, increasing the risk of a crash.
July 17, 2025Vehicle EquipmentNHTSA
Mopar Seats recall
Hazard: A head restraint that does not lock can result in an increased risk of injury to the seat occupant during a crash.