Class I · Most seriousActive recall
Glutathione (MDV)
A reasonable chance it could cause serious harm or death.
Does this affect you?
Check your lot numberLot # 1984345, 1980571, 1981940, Use Before Date: 08/27/2026.
Where it was soldUSA Nationwide
Find the lot number printed on your box or bottle. If it matches — and you take this medicine — call your pharmacist. Don't stop a prescribed medicine on your own.
What happened
Microbial Contamination of Sterile Products - out of specifications results were obtained for bacterial endotoxin.
What to do
- Check the lot number and expiry on your medicine against the recall above.
- Talk to your pharmacist or doctor before changing anything — don't stop on your own.
- Report any problems to FDA MedWatch (1-800-FDA-1088 or fda.gov/medwatch).
Who makes it
| Distributed by / for | Victory Medical Center Pharmacy |
Show the full FDA record
| Full product label | 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. |
| Recalling firm | Victory Medical Center Pharmacy |
| Distribution | USA Nationwide |
| Quantity | 91 |
| Recall initiated | 2026-07-01 |
| Report date | 2026-08-19 |
| Recall completed | — |
| Recall number | D-0772-2026 |
| Classification | Class I |
| FDA status | Ongoing |
| Origin on file | Austin TX United States |
Source: U.S. FDA enforcement database (openFDA). Look this up on the official FDA recalls site ↗
This is public FDA recall information, not medical advice. A recall does not always mean your specific bottle is affected. Never stop a prescribed medicine without asking your pharmacist or doctor.