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FDA recall 99509: Victory Medical Center Pharmacy: Glutathione

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FDARecall 99509Medicines

What to do

The FDA record of this recall has no instruction for consumers. Compare the lot codes below with your product. If they match, do not use it, and follow the notice of the firm or ask the store where you bought it. Talk to your pharmacist or doctor before stopping a medicine.Note from Recalls Watch, not agency text.

Read the official notice on accessdata.fda.gov (opens in a new tab)

Hazard

Why it was recalled

Microbial Contamination of Sterile Products - out of specifications results were obtained for bacterial endotoxin.
Text from FDA, unedited.

FDA classification: Class I. FDA’s highest class: a reasonable probability that using the product will cause serious health consequences or death. Status: Ongoing.

Is it yours? Products and codes

  • 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 or code
    Lot # 1984345, 1980571, 1981940, Use Before Date: 08/27/2026.
    FDA recall number
    D-0772-2026
    Quantity
    91

Distribution (FDA): USA Nationwide

About this record

Issued by
U.S. Food and Drug Administration
Firm
Victory Medical Center Pharmacy
Title
Composed by Recalls Watch from fields of the record; FDA records have no title.

If someone was hurt or swallowed something: call 911, or Poison Help at 1-800-222-1222.

About this recall

What is the hazard?

FDA states: “Microbial Contamination of Sterile Products - out of specifications results were obtained for bacterial endotoxin.”

What should I do if I have this product?

The FDA record of this recall has no instruction for consumers. Compare the lot codes on the notice with your product and follow the notice of the firm. The official report is linked on this page.

How do I know if my product is included?

Compare the lot or code printed on your product with the codes FDA lists on this notice, product by product.

When was this recall published?

FDA published recall 99509 on August 19, 2026.

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