Drug Recalls

Drug Recall Results

Centric Compounding – Compounded Glutathione 200 mg/mL 30 mL multidose vial; Myer’s Cocktail 30 mL multidose vial; Tri-Immune Boost 30 mL multidose vial

Date: 09/13/2026
Company: Centric Compounding LLC
Dosage Form: Other / Unspecified
Recall Issue Type: Quality / Potency
Recall Reason: Elevated Endotoxin level

B. Braun – 0.9% Sodium Chloride Injection USP, 100 mL, in a 150 mL PAB® Container

Date: 09/03/2026
Company: B. Braun Medical Inc.
Dosage Form: Injection
Recall Issue Type: Other Recall Issue
Recall Reason: Presence of particulate matter identified as iron oxide

American Regent, Inc. – Epinephrine Injection, USP 30 mg/ 30 mL (1 mg/mL) multi dose vial

Date: 09/03/2026
Company: American Regent, Inc.
Dosage Form: Injection
Recall Issue Type: Contamination / Sterility
Recall Reason: Presence of particulate matter and lack of sterility assurance

Lipofit – Lipofit Extreme 2.0 Fat Burner Dietary Supplement

Date: 08/31/2026
Company: Ana Salazar Modela Tu Cuerpo Inc.
Dosage Form: Other / Unspecified
Recall Issue Type: Undeclared / Unapproved Ingredient
Recall Reason: Undeclared Fluoxetine and 2,4-Dinitrophenol (DNP)

B. Braun – 0.9% Sodium Chloride Injection USP, 100 mL, in a 150 mL PAB® Container

Date: 08/28/2026
Company: B. Braun Medical Inc.
Dosage Form: Injection
Recall Issue Type: Other Recall Issue
Recall Reason: Presence of particulate matter identified as zinc oxide.

B. Braun – 0.9% Sodium Chloride Injection USP, 100 mL, in a 150 mL PAB® Container

Date: 08/28/2026
Company: B. Braun Medical Inc.
Dosage Form: Injection
Recall Issue Type: Other Recall Issue
Recall Reason: Presence of particulate matter identified as iron oxide

Baxter – 0.9% Sodium Chloride Injection, USP, 500 mL VIAFLEX Plastic Container

Date: 08/26/2026
Company: Baxter International Inc.
Dosage Form: Injection
Recall Issue Type: Other Recall Issue
Recall Reason: Potential presence of particulate matter identified as fiberglass in the solution.

Baxter – Anticoagulant Sodium Citrate Solution USP, 250 mL VIAFLEX Plastic Container

Date: 08/25/2026
Company: Baxter International Inc.
Dosage Form: Solution
Recall Issue Type: Other Recall Issue
Recall Reason: Potential presence of particulate matter identified as fiberglass in the solution

Baxter – 70% Dextrose Injection, USP in 2000 mL VIAFLEX Plastic Container

Date: 08/25/2026
Company: Baxter International Inc.
Dosage Form: Injection
Recall Issue Type: Other Recall Issue
Recall Reason: Potential presence of particulate matter identified as stainless steel particles in the solution.

Vitruvias Therapeutics – Thyroid Tablets, USP 30 mg

Date: 08/24/2026
Company: Vitruvias Therapeutics, Inc
Dosage Form: Tablet
Recall Issue Type: Quality / Potency
Recall Reason: Potential for the Product to be Superpotent

Optimal Balance Pharmacy – Glutathione Injection 200MG/ML (30ML), Multi-Dose Vial

Date: 08/20/2026
Company: Optimal Balance Pharmacy
Dosage Form: Injection
Recall Issue Type: Quality / Potency
Recall Reason: Elevated Endotoxin level

B. Braun – Excel® Lactated Ringers Injection, 1000mL

Date: 08/19/2026
Company: (B. Braun)
Dosage Form: Injection
Recall Issue Type: Other Recall Issue
Recall Reason: Presence of particulate matter identified primarily as cellulose cotton fibers, with individual particles also identified as cellulose wood fiber and polystyrene

Fresenius Kabi – Tyenne Injection 400 mg/20 mL vial

Date: 08/11/2026
Company: Fresenius Kabi
Dosage Form: Injection
Recall Issue Type: Other Recall Issue
Recall Reason: Due to Presence of Glass Particles

VMC – Compounded Glutathione 200 mg/mL Multi-Dose Vials

Date: 08/05/2026
Company: Victory Medical Center Pharmacy
Dosage Form: Other / Unspecified
Recall Issue Type: Quality / Potency
Recall Reason: Elevated Endotoxin level

Fresenius Kabi – Morphine Sulfate Injection USP, Simplist® 2 mg/1 mL

Date: 08/05/2026
Company: Fresenius Kabi
Dosage Form: Injection
Recall Issue Type: Labeling / Packaging
Recall Reason: Due to a label mix-up

OPTIRAY – OPTIRAY Imaging Bulk Package (IBP) 350, 500mL in vial (Ioversol Injection 74% 350 mg iodine/ml)

Date: 08/04/2026
Company: Liebel-Flarsheim Company, LLC
Dosage Form: Injection
Recall Issue Type: Other Recall Issue
Recall Reason: Presence of particulate matter comprising polyethylene and other plastic materials, stainless steel and glass

American Regent, Inc. – Papaverine Hydrochloride Injection, USP 60 mg/ 2 mL

Date: 07/27/2026
Company: American Regent, Inc.
Dosage Form: Injection
Recall Issue Type: Other Recall Issue
Recall Reason: Products were found to contain particulate matter

Baxter – Cefazolin in Dextrose Injection

Date: 07/24/2026
Company: Baxter International Inc.
Dosage Form: Injection
Recall Issue Type: Other Recall Issue
Recall Reason: Particulate matter (cardboard) found in the solution.

Long Grove Pharmaceuticals – Cyclophosphamide for Injection

Date: 07/24/2026
Company: Sunny Pharmtech, Inc.
Dosage Form: Injection
Recall Issue Type: Other Recall Issue
Recall Reason: Presence of particulate matter identified as steel

Rising Pharma Holdings Inc. – Cetirizine Hydrochloride Tablets USP 5 mg

Date: 07/20/2026
Company: Unique Pharmaceutical Laboratories
Dosage Form: Tablet
Recall Issue Type: Contamination / Sterility
Recall Reason: Potential cross contamination with Ranitidine
1 2 3 7