Drug Recalls Drug Recall ResultsAll Dosage FormsCapsule (16)Injection (44)Other / Unspecified (51)Powder (1)Solution (7)Suspension (5)Tablet (23)Topical (2)All Recall CategoriesContamination / Sterility (21)Labeling / Packaging (14)Other Recall Issue (66)Quality / Potency (12)Undeclared / Unapproved Ingredient (34)SearchPar Health and Endo USA – Argatroban Injection 250 mg/2.5 mL (100 mg/mL)Date: 10/14/2026Company: Par Health USA, LLCDosage Form: InjectionRecall Issue Type: Other Recall IssueRecall Reason: Presence of particulate matter, identified as cellulose, polystyrene, polyethylene terephthalate, stopper material, and possibly stainless steelView Full Details →Par Pharmaceutical – Brevital Sodium 500 mg/vial for InjectionDate: 10/09/2026Company: Par HealthDosage Form: InjectionRecall Issue Type: Other Recall IssueRecall Reason: Presence of particulate matter identified as celluloseView Full Details →Greenwich – Glutathione InjectionDate: 10/01/2026Company: Greenwich RxDosage Form: InjectionRecall Issue Type: Quality / PotencyRecall Reason: Potential elevated endotoxin levelsView Full Details →Greewich – Glutathione InjectionDate: 10/01/2026Company: Greenwich RxDosage Form: InjectionRecall Issue Type: Quality / PotencyRecall Reason: Potential elevated endotoxin levelsView Full Details →Par Pharmaceutical – Dexmedetomidine HCl in 0.9% Sodium Chloride Injection 400 mcg/100 mL (4 mcg/mL) for Intravenous InfusionDate: 09/21/2026Company: Par HealthDosage Form: InjectionRecall Issue Type: Other Recall IssueRecall Reason: Presence of particulate matter identified as cellulose or stopper materialView Full Details →Niwali – Tejocote Capsules and PiecesDate: 09/21/2026Company: Global Mix Inc.Dosage Form: CapsuleRecall Issue Type: Other Recall IssueRecall Reason: Products contain yellow oleander (Thevetia peruviana).View Full Details →ICU Medical LLC – 0.9% Sodium Chloride Injection, USP, 100 mLDate: 09/21/2026Company: Otsuka ICU Medical LLCDosage Form: InjectionRecall Issue Type: Other Recall IssueRecall Reason: Product mix-up where 0.9% Sodium Chloride Injection, USP overwrap may contain 10 mEq Potassium Chloride InjectionView Full Details →Centric Compounding – Compounded Glutathione 200 mg/mL 30 mL multidose vial; Myer’s Cocktail 30 mL multidose vial; Tri-Immune Boost 30 mL multidose vialDate: 09/13/2026Company: Centric Compounding LLCDosage Form: Other / UnspecifiedRecall Issue Type: Quality / PotencyRecall Reason: Elevated Endotoxin levelView Full Details →B. Braun – 0.9% Sodium Chloride Injection USP, 100 mL, in a 150 mL PAB® ContainerDate: 09/03/2026Company: B. Braun Medical Inc.Dosage Form: InjectionRecall Issue Type: Other Recall IssueRecall Reason: Presence of particulate matter identified as iron oxideView Full Details →American Regent, Inc. – Epinephrine Injection, USP 30 mg/ 30 mL (1 mg/mL) multi dose vialDate: 09/03/2026Company: American Regent, Inc.Dosage Form: InjectionRecall Issue Type: Contamination / SterilityRecall Reason: Presence of particulate matter and lack of sterility assuranceView Full Details →Lipofit – Lipofit Extreme 2.0 Fat Burner Dietary SupplementDate: 08/31/2026Company: Ana Salazar Modela Tu Cuerpo Inc.Dosage Form: Other / UnspecifiedRecall Issue Type: Undeclared / Unapproved IngredientRecall Reason: Undeclared Fluoxetine and 2,4-Dinitrophenol (DNP)View Full Details →B. Braun – 0.9% Sodium Chloride Injection USP, 100 mL, in a 150 mL PAB® ContainerDate: 08/28/2026Company: B. Braun Medical Inc.Dosage Form: InjectionRecall Issue Type: Other Recall IssueRecall Reason: Presence of particulate matter identified as zinc oxide.View Full Details →B. Braun – 0.9% Sodium Chloride Injection USP, 100 mL, in a 150 mL PAB® ContainerDate: 08/28/2026Company: B. Braun Medical Inc.Dosage Form: InjectionRecall Issue Type: Other Recall IssueRecall Reason: Presence of particulate matter identified as iron oxideView Full Details →Baxter – 0.9% Sodium Chloride Injection, USP, 500 mL VIAFLEX Plastic ContainerDate: 08/26/2026Company: Baxter International Inc.Dosage Form: InjectionRecall Issue Type: Other Recall IssueRecall Reason: Potential presence of particulate matter identified as fiberglass in the solution.View Full Details →Baxter – Anticoagulant Sodium Citrate Solution USP, 250 mL VIAFLEX Plastic ContainerDate: 08/25/2026Company: Baxter International Inc.Dosage Form: SolutionRecall Issue Type: Other Recall IssueRecall Reason: Potential presence of particulate matter identified as fiberglass in the solutionView Full Details →Baxter – 70% Dextrose Injection, USP in 2000 mL VIAFLEX Plastic ContainerDate: 08/25/2026Company: Baxter International Inc.Dosage Form: InjectionRecall Issue Type: Other Recall IssueRecall Reason: Potential presence of particulate matter identified as stainless steel particles in the solution.View Full Details →Vitruvias Therapeutics – Thyroid Tablets, USP 30 mgDate: 08/24/2026Company: Vitruvias Therapeutics, IncDosage Form: TabletRecall Issue Type: Quality / PotencyRecall Reason: Potential for the Product to be SuperpotentView Full Details →Optimal Balance Pharmacy – Glutathione Injection 200MG/ML (30ML), Multi-Dose VialDate: 08/20/2026Company: Optimal Balance PharmacyDosage Form: InjectionRecall Issue Type: Quality / PotencyRecall Reason: Elevated Endotoxin levelView Full Details →B. Braun – Excel® Lactated Ringers Injection, 1000mLDate: 08/19/2026Company: (B. Braun)Dosage Form: InjectionRecall Issue Type: Other Recall IssueRecall Reason: Presence of particulate matter identified primarily as cellulose cotton fibers, with individual particles also identified as cellulose wood fiber and polystyreneView Full Details →Fresenius Kabi – Tyenne Injection 400 mg/20 mL vialDate: 08/11/2026Company: Fresenius KabiDosage Form: InjectionRecall Issue Type: Other Recall IssueRecall Reason: Due to Presence of Glass ParticlesView Full Details →1 2 3 … 8 Next »
