DrugSep 18, 2024
Elevate Oral Care Just Right 5000, 1.1% Sodium Fluoride, Candy Apple Flavor, Net Wt. 3.4oz recall — FDA D-0658-2024
LABELING: LABEL MIX-UP.
Class IIIFDA: TerminatedElevate Oral Care
Monthly breakdown
2024 recalls by month
Select a month to review the recall records reported during that period.
December 202459 records · 2 categoriesNovember 202419 records · 2 categoriesOctober 202418 records · 2 categoriesSeptember 202412 records · 2 categoriesAugust 202417 records · 2 categories
2024 recalls — page 5
Records are ordered by the best available source date.
VehicleSep 13, 2024
F-150 lighting control module recall — NHTSA campaign 24V682000
Ford Motor Company (Ford) is recalling certain 2022 F-150 vehicles. The parking lights may flicker when the headlights are activated. As such, these vehicles fail to comply with the…
lighting control moduleFord Motor Company
VehicleSep 13, 2024
Tucson labels recall — NHTSA campaign 24V691000
Hyundai Motor America (Hyundai) is recalling certain 2025 Tucson vehicles. The glove box air bag warning label may be missing. As such, these vehicles fail to comply with the requirements…
labelsHyundai Motor America
VehicleSep 12, 2024
Jeep Wrangler camera recall — NHTSA campaign 24V676000
Chrysler (FCA US, LLC) is recalling certain 2018-2024 Jeep Wrangler vehicles. The wiring harness for the rearview camera and the center brake light may short circuit, which can disable the…
cameraChrysler (FCA US, LLC)
DrugSep 11, 2024
HEPARIN SODIUM IN SODIUM CHLORIDE Heparin recall — FDA D-0649-2024
Microbial Contamination of Sterile Products; out of limit results obtained for endotoxin testing.
Class IFDA: OngoingBaxter Healthcare Corporation
VehicleSep 5, 2024
Chrysler control unit/module recall — NHTSA campaign 24V653000
Chrysler (FCA US, LLC) is recalling certain 2019, 2021-2024 Ram 1500 vehicles. Due to a software malfunction, the anti-lock brake system (ABS) control module may disable the electronic…
control unit/moduleChrysler (FCA US, LLC)
VehicleSep 5, 2024
Chrysler instrument cluster/panel recall — NHTSA campaign 24V652000
Chrysler (FCA US, LLC) is recalling certain 2020-2024 Jeep Gladiator and 2018-2024 Jeep Wrangler vehicles. The instrument panel cluster may experience an internal short circuit and fail. As…
instrument cluster/panelChrysler (FCA US, LLC)
DrugSep 4, 2024
IBU Ibuprofen Tablets, USP, 600 mg recall — FDA D-0645-2024
Failed impurities/degradation specifications: results for unknown impurity, were 0.13% and 0.11% respectively, exceeding the 0.10% specification limit.
Class IIFDA: OngoingDr. Reddy's Laboratories, Inc.
DrugSep 4, 2024
IBU Ibuprofen Tablets, USP, 400 mg recall — FDA D-0646-2024
Failed impurities/degradation specifications: results for unknown impurity, were 0.13% and 0.11% respectively, exceeding the 0.10% specification limit.
Class IIFDA: OngoingDr. Reddy's Laboratories, Inc.
DrugSep 4, 2024
Cefixime for Oral Suspension USP, 100 mg/5 mL, 50 mL bottle recall — FDA D-0648-2024
Subpotent Drug- An out of specification ( OOS ) result observed in assay test during 18-month long term stability study.
Class IIFDA: TerminatedLupin Pharmaceuticals Inc.
DrugSep 4, 2024
Indomethacin Extended-Release Capsules, USP, 75 mg recall — FDA D-0643-2024
Failed Dissolution Specifications: below specification results
Class IIFDA: OngoingGlenmark Pharmaceuticals Inc., USA
DrugSep 4, 2024
IBU Ibuprofen Tablets, USP, 800 mg recall — FDA D-0644-2024
Failed impurities/degradation specifications: results for unknown impurity, were 0.13% and 0.11% respectively, exceeding the 0.10% specification limit.
Class IIFDA: OngoingDr. Reddy's Laboratories, Inc.
DrugAug 28, 2024
Zeco HAND-I-SAN, No-Rinse Hand Sanitizer (75% Isopropyl Alcohol) recall — FDA D-0640-2024
CGMP Deviations: sterile water not used for production
Class IIFDA: CompletedZeco LLC
DrugAug 28, 2024
Acetaminophen Injection, 1,000 mg per 100 mL (10 mg/mL), 100 mL Single Dose bags, For recall — FDA D-0635-2024
Labeling: Label Mix-up: a bag of Dexmedetomidine HCl in 0.9% Sodium Chloride Injection was found inside an overwrap labeled Acetaminophen Injection 1,000 mg per 100 mL (10 mg/mL)
Class IFDA: OngoingHikma Pharmaceuticals USA Inc.
DrugAug 28, 2024
ACETAMINOPHEN ASPIRIN AND CAFFEINE Healthy Living Acetaminophen, Aspirin (NSAID) and recall — FDA D-0641-2024
Labeling: Missing Label - some bottles are missing the the manufacturers label that includes the drug facts information.
Class IFDA: OngoingAurobindo Pharma USA Inc
DrugAug 28, 2024
Timolol Maleate Ophthalmic Solution USP, 0.5% recall — FDA D-0642-2024
Defective Container: patients are unable to get the solution out of the bottle as the spike of the cap was lodged in the nozzle of the product bottle.
Class IIFDA: OngoingFDC Limited
DrugAug 28, 2024
Zeco Rubbing Alcohol (70% Isopropyl Alcohol), First-Aid Antiseptic recall — FDA D-0639-2024
CGMP Deviations: sterile water not used for production
Class IIFDA: CompletedZeco LLC
VehicleAug 23, 2024
Ford hard parts internal/mechanical recall — NHTSA campaign 24V635000
Ford Motor Company (Ford) is recalling certain 2021-2022 Bronco, F-150, Edge, Explorer, Lincoln Nautilus, and Lincoln Aviator vehicles equipped with either a 2.7L or 3.0L Nano EcoBoost…
hard parts internal/mechanicalFord Motor Company
DrugAug 21, 2024
Timolol Maleate Ophthalmic Solution USP, 0.5%, Sterile, 5mL bottles recall — FDA D-0632-2024
Defective container; yellow colored spike from cap lodged in the nozzle
Class IIFDA: OngoingFDC Limited
DrugAug 21, 2024
Taro Pharmaceuticals U.S.A Hydrocortisone 1% & Acetic Acid 2% Otic Solution, 10 mL bottle recall — FDA D-0633-2024
Failed Impurities/Degradation Specifications: Out-of-specification results obtained for related impurities and slightly lower than the established level of the Hydrocortisone Assay obtained…
Class IIIFDA: CompletedTaro Pharmaceuticals U.S.A., Inc.
DrugAug 14, 2024
Gabapentin Tablets, USP, 600 mg, 500-count bottles recall — FDA D-0634-2024
Presence of Foreign Tablets; 3 fused tablets of Metformin ER 500 mg were found in bottle of Gabapentin Tablets
Class IIFDA: TerminatedGranules Pharmaceuticals Inc.
DrugAug 14, 2024
Sevelamer Carbonate for Oral Suspension 0.8g packets recall — FDA D-0625-2024
Labeling: Incorrect or Missing Lot and/or Exp Date. Missing lot number and expiration dates on packets
Class IIIFDA: OngoingDr. Reddy's Laboratories, Inc.
DrugAug 14, 2024
Amneal Pharmaceuticals Methotrexate Tablets, USP, 2.5mg, 100-count Bottle recall — FDA D-0629-2024
Presence of Foreign Tablets: Potential presence of Fludrocortisone Acetate Tablet USP 0.1 mg within the Methotrexate 2.5 mg 100-count Bottle.
Class IIIFDA: CompletedAmneal Pharmaceuticals, LLC
DrugAug 14, 2024
Acetaminophen Extra Strength Tablets, 500 mg each, 100 count bottles recall — FDA D-0631-2024
Labeling: Label Mix-Up: Some bottles of Acetaminophen Extra Strength 500 mg tablets were incorrectly labeled with the drug facts label for Aspirin 81 mg tablets.
Class IFDA: TerminatedA-S Medication Solutions LLC
About the 2024 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.