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Ongoing FDAEvent 99509 (2 months ago)

Victory Medical Center Pharmacy Glutathione Injection

Compounded glutathione vials have elevated bacterial endotoxin levels, which could cause fever, hypotension, inflammatory reactions, anaphylactic shock.

High risk

There is a reasonable chance that taking it could cause serious health problems or death.

FDA Class I recall · How risk is rated

What to do

What happened

Victory Medical Center Pharmacy, in Austin, Texas, voluntarily recalled certain lots of Compounded Glutathione 200 mg/mL Multi-Dose Vials to the patient level. The recall began July 1, 2026, and was announced August 5, 2026, after pharmacy testing identified elevated bacterial endotoxin levels. The product, Glutathione (MDV), 200 mg/mL, 30 mL vial, contains Glutathione 200 mg, Ascorbic Acid 20 mg, Benzyl Alcohol 1.5%, Na Hydroxide (Ph Adjust) in sterile water for injection, VMC.

The product was distributed nationwide in the USA. The recall was added to the FDA's Enforcement Report and classified on August 19, 2026.

Summary by Recall Canary from the FDA notice.

What to do

If a code on your package matches:

  1. Prescribers and patients with questions regarding this recall can contact Victory Medical Center Pharmacy at (512) 279-0985, Monday through Friday 8:00 a.m.–7:00 p.m., Saturday 9:00 a.m.–5:00 p.m., and Sunday 12:00 p.m.–5:00 p.m. CST.
  2. Stop using the product immediately and quarantine any product subject to this recall.
  3. Contact Victory Medical Center Pharmacy to arrange for retrieval and proper disposition of the recalled product.
  4. Contact their prescribing physician if they have experienced any symptoms or problems that may be related to use of this product.

Is yours affected?

Match the lot code and best-by date listed under your product.

  1. VMC Compounded Glutathione 200 mg/mL

    Lot code
    • 1980571
    • 1981940
    • 1984345
    Best-by
    August 27, 2026
    Dosage form
    Multi-Dose Vial
  2. Glutathione (MDV)

    Strength
    200 mg/mL
    Lot
    • 1984345
    • 1980571
    • 1981940
Label photo

Details

Company began the recall
Sold in

USA Nationwide

Event ID
99509
Recall No.
D-0772-2026
Company
Victory Medical Center PharmacyAustin, Texas
Recall type
Voluntary: Firm initiated
Customers told by
Telephone
  1. Company began the recall

  2. Announced by the company

  3. Listed on Recall Canary

  4. Added to FDA's Enforcement Report · Classified by FDA · In FDA's weekly enforcement report

  5. Summary updated

Summary by Recall Canary, written with AI · summary updated Oct 7, 2026 · primary source: U.S. Food and Drug Administration