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Class I · Most seriousActive recall

Glutathione 200 mg/mL

A reasonable chance it could cause serious harm or death.

Does this affect you?
Check your lot numberLot#: LG342009076, Beyond Use Date: 10/4/26
Where it was soldUSA Nationwide.
Find the lot number printed on your box or bottle. If it matches — and you take this medicine — call your pharmacist. Don't stop a prescribed medicine on your own.

What happened

Microbial Contamination of Sterile Products - out of specifications results were obtained for bacterial endotoxin.

What to do

  1. Check the lot number and expiry on your medicine against the recall above.
  2. Talk to your pharmacist or doctor before changing anything — don't stop on your own.
  3. Report any problems to FDA MedWatch (1-800-FDA-1088 or fda.gov/medwatch).

Who makes it

Distributed by / forOPTIMAL BALANCE PHARMACY
Show the full FDA record
Full product labelGlutathione 200 mg/mL, 30 mL sterile multidose vial, Each vial contains: Glutathione, Ascorbic Acid, Benzyl Alcohol & sterile water for injection, For IM or IV Injection Use Only, RX only, Optimal Balance Pharmacy, 2204 Cypress Creek Pkwy Suite F, Houston, TX 77090
Recalling firmOPTIMAL BALANCE PHARMACY
DistributionUSA Nationwide.
Quantity53 vials
Recall initiated2026-08-05
Report date2026-09-09
Recall completed—
Recall numberD-0851-2026
ClassificationClass I
FDA statusOngoing
Origin on fileHouston TX United States

Related

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Source: U.S. FDA enforcement database (openFDA). Look this up on the official FDA recalls site ↗

This is public FDA recall information, not medical advice. A recall does not always mean your specific bottle is affected. Never stop a prescribed medicine without asking your pharmacist or doctor.