DrugNov 15, 2023
Pfizer 4.2% Sodium Bicarbonate Injection, USP 5 mEq/10 mL (0.5mEq/mL), Glass ABBOJECT Unit recall — FDA D-0100-2024
Presence of Particulate Matter: identified as glass.
Class IFDA: TerminatedPfizer Inc.
Latest records
Latest recalls — page 236
The newest recall records with useful source details are listed here.
DrugNov 15, 2023
Oxybutynin Chloride Extended-Release Tablet USP, 15 mg, 100 count bottles recall — FDA D-0098-2024
Failed Dissolution Specifications-out-of-specification (OOS) test results observed for dissolution at the 6 month long term time point.
Class IIFDA: CompletedZydus Pharmaceuticals (USA) Inc.
DrugNov 15, 2023
LIDOCAINE HYDROCHLORIDE 2% Lidocaine HCl Injection, USP, 100mg/5mL(20mg/mL), Glass ABBOJECT recall — FDA D-0102-2024
Presence of Particulate Matter: identified as glass.
Class IFDA: TerminatedPfizer Inc.
DrugNov 15, 2023
Oxybutynin Chloride Extended-Release Tablet USP, 5 mg, 100 count bottles recall — FDA D-0096-2024
Failed Dissolution Specifications-out-of-specification (OOS) test results observed for dissolution at the 6 month long term time point.
Class IIFDA: CompletedZydus Pharmaceuticals (USA) Inc.
VehicleNov 13, 2023
Honda hard parts internal/mechanical recall — NHTSA campaign 23V751000
Honda (American Honda Motor Co.) is recalling certain 2015-2020 Acura TLX, 2016-2020 Acura MDX, 2016 and 2018-2019 Pilot, 2017 and 2019 Ridgeline, and 2018-2019 Odyssey vehicles. Due to a…
hard parts internal/mechanicalHonda (American Honda Motor Co.)
VehicleNov 9, 2023
Subaru of park/neutral start interlock switch recall — NHTSA campaign 23V755000
Subaru of America, Inc. is recalling certain model year 2021 Crosstrek, 2022 Forester, 2021-2023 Legacy, and Outback vehicles. An insufficient weld may allow water to enter the inhibitor…
park/neutral start interlock switchSubaru of America, Inc.
VehicleNov 9, 2023
Subaru of driveshaft recall — NHTSA campaign 23V754000
Subaru of America, Inc. (Subaru) is recalling certain 2024 Crosstrek, Impreza, 2023-2024 Forester, and 2023 WRX vehicles. The front driveshaft assemblies' outer race may develop cracks and…
driveshaftSubaru of America, Inc.
DrugNov 8, 2023
GlaxoSmithKline Consumer Healthcare Holdings TUMS Antacid, Calcium Carbonate USP 1000 mg recall — FDA D-0077-2024
Presence of Foreign Substance: The foreign material is primarily comprised of glass mineral wool.
Class IIFDA: CompletedGlaxoSmithKline Consumer Healthcare Holdings LLC
DrugNov 8, 2023
GlaxoSmithKline Consumer Healthcare Holdings TUMS Antacid, Calcium Carbonate USP 1000 mg recall — FDA D-0078-2024
Presence of Foreign Substance: The foreign material is primarily comprised of glass mineral wool.
Class IIFDA: CompletedGlaxoSmithKline Consumer Healthcare Holdings LLC
DrugNov 8, 2023
TUMS Antacid, Calcium Carbonate USP 1000 mg, Assorted Fruit flavor, Chewable Tablets recall — FDA D-0075-2024
Presence of Foreign Substance: The foreign material is primarily comprised of glass mineral wool.
Class IIFDA: CompletedGlaxoSmithKline Consumer Healthcare Holdings LLC
DrugNov 8, 2023
Liothyronine Sodium Tablets, USP, 25 mcg, 100-count bottles recall — FDA D-0084-2024
Failed Impurities/Degradation Specifications.
Class IIFDA: TerminatedSUN PHARMACEUTICAL INDUSTRIES Inc.
DrugNov 8, 2023
Strong Iodine Solution U.S.P. (Lugol's Solution) (Iodine 5%), 14 mL Glass Dropper bottle in recall — FDA D-0082-2024
CGMP Deviations: Recall due to the absence of USP CGMP compendial requirements.
Class IIFDA: TerminatedSafecor Health, LLC
DrugNov 8, 2023
Liothyronine Sodium Tablets, USP, 5 mcg, 100-count bottles recall — FDA D-0083-2024
Failed Impurities/Degradation Specifications.
Class IIFDA: TerminatedSUN PHARMACEUTICAL INDUSTRIES Inc.
DrugNov 8, 2023
GYNAZOLE 1 Gynazole-1, (Butoconazole Nitrate) Vaginal Cream USP, 2%, Net Wt 5.8 g per recall — FDA D-0081-2024
Incorrect Product Formulation: Hydrophilic Colloidal Silica was used to manufacture the product rather than Hydrophobic Colloidal Silica as required by the manufacturing process.
Class IIFDA: OngoingPadagis US LLC
DrugNov 8, 2023
TUMS Antacid, Calcium Carbonate USP 1000 mg, Peppermint flavor, chewable tablets recall — FDA D-0074-2024
Presence of Foreign Substance: The foreign material is primarily comprised of glass mineral wool.
Class IIFDA: CompletedGlaxoSmithKline Consumer Healthcare Holdings LLC
DrugNov 8, 2023
TUMS Antacid, Calcium Carbonate USP 1000 mg, Assorted Berries flavor, chewable tablets recall — FDA D-0079-2024
Presence of Foreign Substance: The foreign material is primarily comprised of glass mineral wool.
Class IIFDA: CompletedGlaxoSmithKline Consumer Healthcare Holdings LLC
DrugNov 8, 2023
TUMS Antacid, Calcium Carbonate USP 1000 mg, Peppermint flavor, chewable tablets, 72-count recall — FDA D-0073-2024
Presence of Foreign Substance: The foreign material is primarily comprised of glass mineral wool.
Class IIFDA: CompletedGlaxoSmithKline Consumer Healthcare Holdings LLC
DrugNov 8, 2023
GlaxoSmithKline Consumer Healthcare Holdings TUMS Antacid, Calcium Carbonate USP 1000 mg recall — FDA D-0076-2024
Presence of Foreign Substance: The foreign material is primarily comprised of glass mineral wool.
Class IIFDA: CompletedGlaxoSmithKline Consumer Healthcare Holdings LLC
VehicleNov 3, 2023
Tesla steering wheel/handle bar recall — NHTSA campaign 23V743000
Tesla, Inc. (Tesla) is recalling certain 2021-2024 Model S and Model X vehicles. An incorrect air bag may have been installed when the steering yoke or round steering wheel was replaced…
steering wheel/handle barTesla, Inc.
DrugNov 1, 2023
Methotrexate Tablets, USP, 2.5 mg, 10x10 Unit-Dose Tablets per carton recall — FDA D-0066-2024
Failed Tablet/Capsule Specifications: Tablets were observed to have an unsmooth surface with two tablets demonstrating illegible tablet identification and scoring.
Class IIIFDA: OngoingWest-Ward Columbus Inc.
DrugNov 1, 2023
Biomic Sciences, LLC dba ION Intelligence of ION* Sinus Support Nasal Spray, 1 fl oz/30 ml recall — FDA D-0068-2024
Microbial contamination of Non-Sterile Products
Class IIFDA: TerminatedBiomic Sciences, LLC dba ION Intelligence of Nature
VehicleOct 27, 2023
Mustang body control module/bcm recall — NHTSA campaign 23V727000
Ford Motor Company (Ford) is recalling certain 2020-2023 Mustang vehicles. The brake fluid level sensor may not activate the visual warning indicator when the brake fluid is low. As such,…
body control module/bcmFord Motor Company
VehicleOct 26, 2023
Highlander & Highlander Hybrid bumpers recall — NHTSA campaign 23V720000
Toyota Motor Engineering & Manufacturing (Toyota) is recalling certain 2020-2023 Highlander & Highlander Hybrid vehicles. During normal vehicle operation, minor impact to the front lower…
bumpersToyota Motor Engineering & Manufacturing
VehicleOct 26, 2023
Forester engine and engine cooling recall — NHTSA campaign 23V723000
Subaru of America, Inc. (Subaru) is recalling certain 2024 Forester vehicles. The engine water pipe may have loose attachment bolts, allowing the pipe to lose its seal and leak coolant.
engine and engine coolingSubaru of America, Inc.
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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 2025389 records · 4 categoriesNovember 2025326 records · 4 categoriesOctober 2025455 records · 4 categoriesSeptember 2025180 records · 4 categories