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.
Latest records
Latest recalls — page 217
The newest recall records with useful source details are listed here.
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
DrugAug 14, 2024
Empower Pharmacy, Estradiol Cypionate Injection, 10mg/mL, 5mL Sterile Multiple Dose Vial recall — FDA D-0630-2024
Lack of Assurance of Sterility
Class IIFDA: TerminatedEMPOWER CLINIC SERVICES LLC
DrugAug 14, 2024
PEG-3350, Sodium Sulfate, Sodium Chloride, Potassium Chloride, Sodium Ascorbate, and recall — FDA D-0628-2024
Defective container: potential for non-sealed pouches which can lead to product leakage.
Class IIIFDA: TerminatedNovel Laboratories, Inc. d.b.a Lupin Somerset
DrugAug 14, 2024
Granules Consumer Health Acetaminophen, USP 500mg, Pain Reliever/Fever Reducer, Extra recall — FDA D-0627-2024
Label mix-up: Carton incorrectly labeled.
Class IIIFDA: TerminatedGranules Consumer Health Inc.
VehicleAug 10, 2024
Explorer engine recall — NHTSA campaign 24V598000
Ford Motor Company (Ford) is recalling certain 2020-2022 Explorer vehicles equipped with the Police Interceptor Utility Package. In the event of an engine failure, engine oil and fuel vapor…
engineFord Motor Company
VehicleAug 9, 2024
Maverick body control module/bcm recall — NHTSA campaign 24V590000
Ford Motor Company (Ford) is recalling certain 2022 Maverick vehicles previously repaired under recall number 24V-267. The body and power train control modules may fail to detect a change…
body control module/bcmFord Motor Company
VehicleAug 9, 2024
Ford motor recall — NHTSA campaign 24V594000
Ford Motor Company (Ford) is recalling certain 2023-2024 Maverick, Ford Bronco Sport, and Mustang Mach-E vehicles. The front windshield wiper motor may become inoperative, causing the…
motorFord Motor Company
VehicleAug 9, 2024
Mustang rear recall — NHTSA campaign 24V593000
Ford Motor Company (Ford) is recalling certain 2024 Mustang vehicles. The rear suspension knuckles may have a casting defect that causes them to fail, which can result in a loss of vehicle…
rearFord Motor Company
VehicleAug 8, 2024
Jeep Wrangler tail lights recall — NHTSA campaign 24V585000
Chrysler (FCA US, LLC) is recalling certain 2024 Jeep Wrangler vehicles. The vehicles are equipped with incorrect tail lights that may be obstructed by the spare tire. As such, these…
tail lightsChrysler (FCA US, LLC)
VehicleAug 7, 2024
Hyundai Sonata brake lights recall — NHTSA campaign 24V583000
Hyundai Motor America (Hyundai) is recalling certain 2024 Hyundai Sonata vehicles. The software for the brake lights may cause the brake lights to flash and not illuminate properly. As…
brake lightsHyundai Motor America
DrugAug 7, 2024
Ciprofloxacin ophthalmic solution USP, 0.3% as base, package in bottles: a) 10 mL recall — FDA D-0623-2024
Defective container: 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 7, 2024
Clonazepam Orally Disintegrating Tablets, USP (C-IV) 0.125mg, 60 tablets per carton recall — FDA D-0622-2024
Labeling: Label Error on Declared Strength; Some cartons were incorrectly labeled as 0.125 mg instead of 0.25 mg. The blister strips inside the product carton reflect the correct strength…
Class IFDA: TerminatedEndo Pharmaceuticals, Inc.
DrugAug 7, 2024
Potassium Chloride Extended-Release Capsules, USP, (750 mg) 10 mEq K, a).100-count bottle recall — FDA D-0619-2024
Failed Dissolution Specifications
Class IFDA: OngoingAmerisource Health Services LLC
DrugAug 7, 2024
Progesterone Injection, USP, 500 mg per 10 mL (50mg/mL), 10 mL Multiple-Dose Vial recall — FDA D-0624-2024
Presence of Particulate Matter: Complaint received of a glass particle in the vial.
Class IIFDA: OngoingEugia US LLC
VehicleAug 6, 2024
Nissan Frontier headlights recall — NHTSA campaign 24V582000
Nissan North America, Inc. (Nissan) is recalling certain 2024 Nissan Frontier vehicles. The right-side headlight assemblies may have missing or illegible headlight aim markings, which can…
headlightsNissan North America, Inc.
VehicleAug 1, 2024
General Motors owners/service/other manual recall — NHTSA campaign 24V575000
General Motors, LLC (GM) is recalling certain 2024 Cadillac XT4 and Chevrolet Malibu vehicles. The vehicles may have the wrong owner's manual in the glove box. As such, these vehicles fail…
owners/service/other manualGeneral Motors, LLC
VehicleAug 1, 2024
Chrysler control module software recall — NHTSA campaign 24V572000
Chrysler (FCA US, LLC) is recalling certain 2021 Jeep Wrangler and Jeep Gladiator vehicles that were previously remedied under NHTSA recall number 23V-116. The software for the powertrain…
control module softwareChrysler (FCA US, LLC)
VehicleAug 1, 2024
BMW starter motor recall — NHTSA campaign 24V576000
BMW of North America, LLC is recalling certain 2019-2020 X5, X7, 2020 3 Series Sedan, X6, 2020-2021 7 Series Sedan, 2020 8 Series Convertible, 8 Series Coupe, and 2020 8 Series Gran Coupe…
starter motorBMW of North America, LLC
DrugJul 31, 2024
GLOBAL WIDGET Hemp Bombs CBD Pain Freeze (menthol 4%), 100mg, 1 oz bottles recall — FDA D-0613-2024
Subpotent drug: The potency of the active (menthol) was less than the label claim of 4%.
Class IIIFDA: OngoingGLOBAL WIDGET LLC
DrugJul 31, 2024
GLOBAL WIDGET Hemp Bombs CBD Pain Freeze (menthol 4%), 1000mg, 4 oz bottles recall — FDA D-0616-2024
Subpotent drug: The potency of the active (menthol) was less than the label claim of 4%.
Class IIIFDA: OngoingGLOBAL WIDGET LLC
DrugJul 31, 2024
GLOBAL WIDGET Nature's Script CBD Cryotherapy Pain Relief Roll on (menthol 4%) 200mg, 1 oz recall — FDA D-0614-2024
Subpotent drug: The potency of the active (menthol) was less than the label claim of 4%.
Class IIIFDA: OngoingGLOBAL WIDGET LLC
DrugJul 31, 2024
GLOBAL WIDGET Hemp Bombs CBD Pain Freeze (menthol 4%), 400mg, 4 oz bottles recall — FDA D-0615-2024
Subpotent drug: The potency of the active (menthol) was less than the label claim of 4%.
Class IIIFDA: OngoingGLOBAL WIDGET LLC
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Recent recall archives
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August 2026149 records · 4 categoriesJuly 2026371 records · 4 categoriesJune 2026375 records · 4 categoriesMay 2026340 records · 4 categoriesApril 2026415 records · 4 categoriesMarch 2026190 records · 4 categoriesFebruary 2026331 records · 4 categoriesJanuary 2026212 records · 4 categoriesDecember 2025388 records · 4 categoriesNovember 2025325 records · 4 categoriesOctober 2025454 records · 4 categoriesSeptember 2025180 records · 4 categories