FDA Drug recall D-0772-2026
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 A…
- FDA Drug
- Class I
- ongoing
- Published 2026-08-19
On 2026-08-19 the FDA classified a Class I recall of 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 A… by Victory Medical Center Pharmacy, citing microbial Contamination of Sterile Products - out of specifications results were obtained for bacterial endotoxin.
Read the official FDA Drug notice
| Agency | FDA Drug |
|---|---|
| Recall number | D-0772-2026 |
| Classification | Class I |
| Status | ongoing |
| Initiated | 2026-07-01 |
| Published | 2026-08-19 |
| Last updated | 2026-09-13 11:52 UTC |
| Company | Victory Medical Center Pharmacy |
| Distribution | US |
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
Microbial Contamination of Sterile Products - out of specifications results were obtained for bacterial endotoxin.
Identifiers
| code_info | Lot # 1984345, 1980571, 1981940, Use Before Date: 08/27/2026. |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:52 UTC. Current status: ongoing.
Source
Official record: https://api.fda.gov/drug/enforcement.json?search=recall_number:%22D-0772-2026%22
RecallRadar indexes public recall notices from the FDA, USDA FSIS, and CPSC. The official agency notice is the authoritative source. Always confirm details at the linked source before acting.