Drug recalls (page 8)
748 recalls.
- MOTRIN 2'S DISP.- 50CT recall (GOLD STAR DISTRIBUTION INC)
DrugClass IIReported January 21, 2026 · CGMP Deviations: Insanitary conditions including rodent exposure/activity in their distribution center. - EXCEDRIN MIGRAINE 2'S- 25 CT recall (GOLD STAR DISTRIBUTION INC)
DrugClass IIReported January 21, 2026 · CGMP Deviations: Insanitary conditions including rodent exposure/activity in their distribution center. - EXCEDRIN 2'S DISP.- 30 CT recall (GOLD STAR DISTRIBUTION INC)
DrugClass IIReported January 21, 2026 · CGMP Deviations: Insanitary conditions including rodent exposure/activity in their distribution center. - LIQUID DAYQUIL 12/8oz recall (GOLD STAR DISTRIBUTION INC)
DrugClass IIReported January 21, 2026 · CGMP Deviations: Insanitary conditions including rodent exposure/activity in their distribution center. - DAYQUIL COLD & FLU recall (GOLD STAR DISTRIBUTION INC)
DrugClass IIReported January 21, 2026 · CGMP Deviations: Insanitary conditions including rodent exposure/activity in their distribution center. - Claritin recall (GOLD STAR DISTRIBUTION INC)
DrugClass IIReported January 21, 2026 · CGMP Deviations: Insanitary conditions including rodent exposure/activity in their distribution center. - Bayer 2Pk- 25 CT recall (GOLD STAR DISTRIBUTION INC)
DrugClass IIReported January 21, 2026 · CGMP Deviations: Insanitary conditions including rodent exposure/activity in their distribution center. - Benadryl recall (GOLD STAR DISTRIBUTION INC)
DrugClass IIReported January 21, 2026 · CGMP Deviations: Insanitary conditions including rodent exposure/activity in their distribution center. - Alka Seltzer recall (GOLD STAR DISTRIBUTION INC)
DrugClass IIReported January 21, 2026 · CGMP Deviations: Insanitary conditions including rodent exposure/activity in their distribution center. - Aleve 1's recall (GOLD STAR DISTRIBUTION INC)
DrugClass IIReported January 21, 2026 · CGMP Deviations: Insanitary conditions including rodent exposure/activity in their distribution center. - Advil a) Ibuprofen recall (GOLD STAR DISTRIBUTION INC)
DrugClass IIReported January 21, 2026 · CGMP Deviations: Insanitary conditions including rodent exposure/activity in their distribution center. - AQ 120 GFEW recall (Encon Safety Products Co)
DrugClass IIReported January 21, 2026 · cGMP deviations. - Levothyroxine Sodium Tablets recall (Alvogen, Inc)
DrugClass IIReported January 21, 2026 · Product Mix-Up: A single bottle of this lot was reported by a pharmacy to contain 88 mcg tablets instead of 150 mcg tablets. - Clindamycin Phosphate USP recall (SUN PHARMACEUTICAL INDUSTRIES INC)
DrugClass IIIReported January 21, 2026 · Failed Impurities/Degradation: Out of Specification results for Total Impurities and for Assay. - Fluocinolone Acetonide Solution Topical Solution USP recall (SUN PHARMACEUTICAL INDUSTRIES INC)
DrugClass IIIReported January 21, 2026 · Failed Impurities/Degradation Specifications: Out of specification result was obtained for the known impurity D. - Rosuvastatin Tablets recall (AvKARE)
DrugClass IIReported January 14, 2026 · Out of specification for dissolution. - ClearLife Allergy Nasal Spray recall (Medinatura New Mexico, inc.)
DrugClass IReported January 14, 2026 · Microbial Contamination of Non-Sterile Products: The products have been found to contain yeast/mold and microbial contamination identified as Achromobacter. - ReBoost Nasal Spray recall (Medinatura New Mexico, inc.)
DrugClass IReported January 14, 2026 · Microbial Contamination of Non-Sterile Products: The products have been found to contain yeast/mold and microbial contamination identified as Achromobacter. - Oxycodone and Acetaminophen CII Tablets USP recall (SpecGx, LLC)
DrugClass IIReported January 14, 2026 · Failed Tablet/Capsule Specification: There is a potential for the imprint to be missing on tablets. - Oxycodone and Acetaminophen CII Tablets USP recall (SpecGx, LLC)
DrugClass IIReported January 14, 2026 · Failed Tablet/Capsule Specification: There is a potential for the imprint to be missing on tablets. - ORL Kids Natural Toothpaste recall (Signature Formulations, LLC)
DrugClass IIReported January 14, 2026 · cGMP Deviations - ORL Kids Mouthwash recall (Signature Formulations, LLC)
DrugClass IIReported January 14, 2026 · cGMP Deviations - Tri-Moxi+¿ recall (Imprimis NJOF, LLC)
DrugClass IIReported January 14, 2026 · Presence of particulate matter - Glass like particles. - Dexamethasone Moxifloxacin Ketorolac recall (Imprimis NJOF, LLC)
DrugClass IIReported January 14, 2026 · Presence of particulate matter - Glass like particles. - Dexamethasone Moxifloxacin recall (Imprimis NJOF, LLC)
DrugClass IIReported January 14, 2026 · Presence of particulate matter - Glass like particles. - Fesoterodine Fumarate recall (Alembic Pharmaceuticals Limited)
DrugClass IIIReported January 14, 2026 · Failed Impurities/Degradation Specifications: Due to levels of 'Diester Impurity' exceeding the specification limit. - traZODONE Hydrochloride Tablets recall (Zydus Pharmaceuticals (USA) Inc)
DrugClass IIIReported January 7, 2026 · Failed Tablet/Capsule Specifications: Product complaint received that some tablets had a dent on the plain side of the tablet surface. - Ondansetron Orally Disintegrating Tablets recall (Glenmark Pharmaceuticals Inc., USA)
DrugClass IIReported January 7, 2026 · Defective container: Preferred Pharmaceuticals received a letter from the manufacturer Glenmark, that the blister packs are not fully sealed and tablets... - Wegovy recall (Novo Nordisk Inc.)
DrugClass IIReported January 7, 2026 · Presence of Particulate Matter: Hair was found in a prefilled syringe - Wegovy recall (Novo Nordisk Inc.)
DrugClass IIReported January 7, 2026 · Presence of Particulate Matter: Hair was found in a prefilled syringe - BD ChloraPrep" Triple Swabsticks recall (CareFusion 213, LLC)
DrugClass IIReported January 7, 2026 · Lack of Assurance of Sterlity - Noxafil Powdermix recall (Merck Sharp & Dohme LLC)
DrugClass IIReported December 31, 2025 · Presence of particulate matter: potential presence of metal particulates in the product. - Merck Emend recall (Merck Sharp & Dohme LLC)
DrugClass IIReported December 31, 2025 · Presence of particulate matter: potential presence of metal particulates in the product. - Ciclopirox Shampoo recall (SUN PHARMA /TARO)
DrugClass IIReported December 24, 2025 · Failed Impurity/Degradation specifications: OOS results obtained at the 18-month timepoint - Ondansetron ODT Tablets recall (Preferred Pharmaceuticals, Inc.)
DrugClass IIReported December 24, 2025 · Defective container: Preferred Pharmaceuticals received a letter from the manufacturer Glenmark, that the blister packs are not fully sealed and tablets... - Cisatracurium Besylate Injection USP recall (SOMERSET THERAPEUTICS LLC)
DrugClass IIIReported December 24, 2025 · Subpotent product:out of specification assay results observed during long term stability testing. - Cisatracurium Besylate Injection USP recall (SOMERSET THERAPEUTICS LLC)
DrugClass IIIReported December 24, 2025 · Subpotent product:out of specification assay results observed during long term stability testing. - Cisatracurium Besylate Injection USP recall (SOMERSET THERAPEUTICS LLC)
DrugClass IIIReported December 24, 2025 · Subpotent product:out of specification assay results observed during long term stability testing. - Baclofen Tablets USP recall (Golden State Medical Supply Inc.)
DrugClass IIReported December 24, 2025 · Presence of Foreign Tablets/Capsules - Cinacalcet Hydrochloride Tablets recall (Cipla USA, Inc.)
DrugClass IIReported December 17, 2025 · CGMP Deviations: the presence of a nitrosamine impurity, N-nitroso-cinacalcet, above the acceptable daily intake (ADI) limits. - Cinacalcet Hydrochloride Tablets recall (Cipla USA, Inc.)
DrugClass IIReported December 17, 2025 · CGMP Deviations: the presence of a nitrosamine impurity, N-nitroso-cinacalcet, above the acceptable daily intake (ADI) limits. - Cinacalcet Hydrochloride Tablets recall (Cipla USA, Inc.)
DrugClass IIReported December 17, 2025 · CGMP Deviations: the presence of a nitrosamine impurity, N-nitroso-cinacalcet, above the acceptable daily intake (ADI) limits. - Morphine Sulfate Oral Solution 100 mg / 5 mL recall (Winder Laboratories, LLC)
DrugClass IIIReported December 17, 2025 · Correct Labeled Product Mispack-Size stated on carton label did not match the size of the bottle in the carton. - Nebivolol Tablets recall (Glenmark Pharmaceuticals Inc., USA)
DrugClass IIIReported December 17, 2025 · Cross Contamination with Other Products - Tropicamide 1%/Cyclopentolate 1%/Phenylephrine 2.5%/Ketorolac 0.5% Topical Ophthalmic... recall (Fagron Compounding Services)
DrugClass IIReported December 17, 2025 · Incorrect Product Formulation - Duloxetine Delayed-Release Capsules recall (Breckenridge Pharmaceutical, Inc.)
DrugClass IIReported December 10, 2025 · CGMP Deviations; presence of N-nitroso-duloxetine impurity above the FDA recommended limit - Duloxetine Delayed-Release Capsules recall (Breckenridge Pharmaceutical, Inc.)
DrugClass IIReported December 10, 2025 · CGMP Deviations; presence of N-nitroso-duloxetine impurity above the FDA recommended limit - Bisoprolol Fumarate and Hydrochlorothiazide Tablets recall (Glenmark Pharmaceuticals Inc., USA)
DrugClass IIIReported December 10, 2025 · Cross Contamination with Other Products: Testing of reserve samples showed presence of traces of ezetimibe