CLASS I ONGOING Drug recall · Reported 19 Aug 2026 · FDA Enforcement Report
Glutathione (MDV), 200 mg/mL vial recalled by Victory Medical Center
Victory Medical Center Pharmacy is recalling Glutathione (MDV), 200 mg/mL vial, each mL contains Glutathione 200 mg, Ascorbic Acid 20, distributed nationwide in the US. The recall was initiated on 1 Jul 2026 and the FDA has classified it as Class I.
Check your package
Check the lot number on your package against the affected lots. If it matches, contact the pharmacy that dispensed it or your prescriber before stopping any medication.
Recall details
- Recall number
- D-0772-2026
- FDA event ID
- 99509
- Recalling firm
- Victory Medical Center Pharmacy, Austin, TX
- Classification
- Class I
- Status
- Ongoing
- Recall initiated
- 1 Jul 2026
- FDA classified
- 19 Aug 2026
- Reported
- 19 Aug 2026
- Type
- Voluntary: Firm initiated
- Customers notified by
- Telephone
- Reason category
- Sterility
- Drug class
- Injectable & IV Drugs
Timeline
| 1 Jul 2026 | Recall initiated by company | |
| 19 Aug 2026 | Classified by FDA | +49 days |
| 19 Aug 2026 | Published in enforcement report | +0 days |
Companies usually start a recall weeks before the FDA classifies and publishes it; the gap above is that lag.
Reason for recall
Microbial Contamination of Sterile Products - out of specifications results were obtained for bacterial endotoxin.
A sterility recall means a product that must be sterile, such as an injection or eye drop, may be contaminated. Using a non-sterile product can cause serious infection.
Product as listed by the FDA
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.
Where it was distributed
USA Nationwide
Questions about this recall
Why was it recalled?
Microbial Contamination of Sterile Products - out of specifications results were obtained for bacterial endotoxin.
Which lots are affected?
Lot # 1984345, 1980571, 1981940, Use Before Date: 08/27/2026.
Where was it sold?
USA Nationwide
What should I do if I have it?
Check the lot number on your package against the affected lots. If it matches, contact the pharmacy that dispensed it or your prescriber before stopping any medication.
What does Class I mean?
Class I is the most serious FDA recall category: there is a reasonable probability that using the product will cause serious health consequences or death.
Read the official FDA notice · Source record retrieved 26 Sep 2026. The FDA describes openFDA data as unvalidated; the official notice takes precedence. This page reports the record and gives no medical advice.
Other Glutathione (mdv recalls
All 2| Reported | Class | Recall | Company | Reason | Where |
|---|---|---|---|---|---|
| Drug | CLASS II | Glutathione MDV, Injectable Solution, 200 mg/mL, syringe sizes recalled | JD & SN Inc | Sterility | Nationwide |