Glutathione (MDV), 200 mg/mL, 30 mL vial, each mL contains… was recalled on July 1, 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..
Glutathione (MDV), 200 mg/mL, 30 mL vial, each mL contains Glutathione 200 mg, Ascorbic Acid 20 mg, Benzyl Alcohol 1.5%, Na Hydroxide (Ph Adjust) in sterile water for injection, VMC.
Lot # 1984345, 1980571, 1981940, Use Before Date: 08/27/2026.
Units affected: 91
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.
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.
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: Victory Medical Center Pharmacy
Not sure what you're entitled to? Read our guide: what to do if your product is recalled.
Always confirm details on the official notice from the U.S. Food and Drug Administration before acting.
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