FDAFDA recall D-0772-2026 · Aug 19, 2026
Victory Medical Center Pharmacy: Glutathione (MDV) recall
Recall found
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.
Reason for recall
Microbial Contamination of Sterile Products - out of specifications results were obtained for bacterial endotoxin.
What to do
FDA enforcement reports don't include consumer instructions. Check the codes below against your packaging. If this is a medicine or device you use, talk to your pharmacist or doctor before you stop or change anything, and contact the company or FDA for what to do with the product.
Recall details
- FDA classification
- Class I: FDA's most serious class, where use of or exposure to the product may cause serious health problems or death.
- Status
- Ongoing
- Codes, lots and dates
- Lot # 1984345, 1980571, 1981940, Use Before Date: 08/27/2026.
- Quantity
- 91
- Distribution
- USA Nationwide
- Recalling firm
- Victory Medical Center Pharmacy, Austin, TX
- Voluntary or mandated
- Voluntary: Firm initiated
- Recall started
- 2026-07-01
Source: openFDA enforcement record D-0772-2026 · search recall number D-0772-2026 in FDA's Enforcement Report.
Copied from the agency record without changes. Data as of Oct 22, 2026, 4:56 AM EDT. The agency notice is the final word.