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FDAClass I

Glutathione 200 mg/mL, 30 mL sterile multidose vial, Each vial contains: Glutathione, Asc… Recalled: Microbial Contamination of Sterile Products - out of specifications results were obtained…

Glutathione 200 mg/mL, 30 mL sterile multidose vial, Each… was recalled on August 5, 2026 in cooperation with the U.S. Food and Drug Administration because microbial Contamination of Sterile Products - out of specifications results were obtained for bacterial endotoxin..

Is my unit affected?

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

Model, lot & date codes to check

Lot#: LG342009076, Beyond Use Date: 10/4/26

Units affected: 53 vials

Where it was sold: USA Nationwide.

Compare the codes above against the label on your product — usually on the bottom, the back panel, or the packaging. If your unit isn't listed, it is not part of this recall.

What's the hazard?

Microbial Contamination of Sterile Products - out of specifications results were obtained for bacterial endotoxin.

Class I is the most serious FDA recall level: using or being exposed to the product could cause serious health problems or death.

Your remedy & how to claim it

Stop using the product. Return it to the place of purchase for a refund, or dispose of it. Contact the recalling firm with questions.

Contact: Recalling firm: OPTIMAL BALANCE PHARMACY

Not sure what you're entitled to? Read our guide: what to do if your product is recalled.

Official recall notice

Always confirm details on the official notice from the U.S. Food and Drug Administration before acting.

View official notice →

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