FDA Drugs recall ·
Glutathione (MDV), 200 mg/mL, 30 mL vial, each mL contains Glutathione 200… recall
This is an FDA Class I recall — the most serious type.
- Recall number
- D-0772-2026
- Date
- (initiated July 1, 2026)
- Company / brand
- Victory Medical Center Pharmacy
4303 Victory Dr, Austin, TX, United States - Category
- Drugs › Class I
- Classification
- Class I
- Status
- Ongoing
- Units affected
- 91
- Hazard tags
- Sterility Microbial contamination
- Initiated by
- Voluntary: Firm initiated
Read the official FDA notice ↗
Product
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.
Why was it recalled?
Microbial Contamination of Sterile Products - out of specifications results were obtained for bacterial endotoxin.
What should you do?
FDA enforcement reports do not list a consumer remedy. Check the product codes below against what you have; if it matches, stop using it and follow the instructions in the firm's or FDA's official notice, or contact the company. If you have health concerns, contact your healthcare provider.
Product codes & lot numbers
Lot # 1984345, 1980571, 1981940, Use Before Date: 08/27/2026.
Distribution
USA Nationwide
What does Class I mean?
Class I is the most serious FDA recall class: there is a reasonable probability that using or being exposed to the product will cause serious adverse health consequences or death.
Source: FDA (drugs), recall D-0772-2026. Official notice. Republished from public data; RecallFlag is not affiliated with the FDA.