Why it was recalled
Microbial Contamination of Sterile Products - out of specifications results were obtained for bacterial endotoxin.
Product description
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.
Lot numbers, UPCs & expiration codes
Lot # 1984345, 1980571, 1981940, Use Before Date: 08/27/2026.
Where it was sold
USA Nationwide
What to do if you have this product
- Compare the lot number and expiration date on your package with the codes above.
- Don't stop taking a prescription medicine on your own. Call your pharmacist or doctor; they can confirm whether your supply is affected and arrange a replacement.
- If you have symptoms you think are related, contact your doctor. In an emergency call 911.
- Report side effects to FDA MedWatch at 1-800-FDA-1088.
Recall details
- Recall number
- D-0772-2026
- Classification
- Class I
- Status
- Ongoing
- Recall initiated
- Jul 1, 2026
- FDA report date
- Aug 19, 2026
- Quantity
- 91
- Recall type
- Voluntary: Firm initiated
- Recalling firm
- Victory Medical Center Pharmacy
Original FDA data
Every field from FDA enforcement report D-0772-2026, exactly as published.
Show all FDA fields
- City
- Austin
- State
- TX
- Status
- Ongoing
- Country
- United States
- Event ID
- 99509
- Address
- 4303 Victory Dr
- Code information
- Lot # 1984345, 1980571, 1981940, Use Before Date: 08/27/2026.
- Postal code
- 78704-7507
- Report date
- Aug 19, 2026
- Product type
- Drugs
- Recall number
- D-0772-2026
- Classification
- Class I
- Recalling firm
- Victory Medical Center Pharmacy
- Product quantity
- 91
- Reason for recall
- Microbial Contamination of Sterile Products - out of specifications results were obtained for bacterial endotoxin.
- Voluntary / mandated
- Voluntary: Firm initiated
- Product description
- 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.
- Distribution pattern
- USA Nationwide
- Recall initiation date
- Jul 1, 2026
- Initial firm notification
- Telephone
- Center classification date
- Aug 19, 2026