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Home › FDA recalls › Glutathione 200 mg/mL
CLASS I · SeriousFDA

OPTIMAL BALANCE PHARMACY recalls Glutathione 200 mg/mL

📅 Aug 5, 2026 · 📍 Nationwide
Recalling company
OPTIMAL BALANCE PHARMACY
Product
Glutathione 200 mg/mL, 30 mL sterile multidose vial, Each vial contains: Glutathione, Ascorbic Acid, Benzyl Alcohol & sterile water for injection, For IM or IV Injection Use Only, RX only, Optimal Balance Pharmacy, 2204 Cypress Creek Pkwy Suite F, Houston, TX 77090
Reason
Microbial Contamination of Sterile Products - out of specifications results were obtained for bacterial endotoxin.
Classification
Class I – a reasonable probability that use will cause serious adverse health consequences or death
Recall date
Aug 5, 2026
Reported
Sep 9, 2026
Distribution
USA Nationwide.
Status
Ongoing
Quantity
53 vials
Lot / codes
Lot#: LG342009076, Beyond Use Date: 10/4/26
Company location
Houston, TX
Recall type
Voluntary: Firm initiated
Recall number
D-0851-2026
Agency
U.S. Food and Drug Administration (FDA)

View official FDA notice ↗ Search recall number D-0851-2026 in the FDA Enforcement Report. Also see FDA recall press releases.

If you use this product, check the lot, NDC or model number against the official notice and follow its instructions. Do not stop a prescribed medicine or remove a medical device without talking to your doctor or pharmacist. Report problems to FDA MedWatch. FoodRecallNow summarizes public FDA data and is not medical advice.