RECALL DATABASE

Glutathione Recall: Optimal Balance Pharmacy 200 mg/mL 30 mL vial

Announced 2026-09-09 · FDA

FDA recall of OPTIMAL BALANCE PHARMACY Glutathione 200 mg/mL, 30 mL sterile multidose vial (Rx only) distributed nationwide in the USA. The issue is microbial contamination with out-of-specification results for bacterial endotoxin. Affected lot LG342009076 has a Beyond Use Date of 10/4/26, and 53 vials were distributed nationwide.

BrandOPTIMAL BALANCE PHARMACY
ProductGlutathione 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
ReasonMicrobial Contamination of Sterile Products - out of specifications results were obtained for bacterial endotoxin.
Severitycritical
Units affected53
DistributionUSA Nationwide.
AgencyFDA

WHAT YOU SHOULD DO

  1. Do not use any recalled vials.
  2. If you have a vial from Lot LG342009076 with Beyond Use Date 10/4/26, stop using it.
  3. Contact your pharmacist or OPTIMAL BALANCE PHARMACY for instructions on return or replacement.
  4. If you have used the product or are concerned, contact your healthcare provider.

How to identify the recalled item

Lot / date codesLot#: LG342009076, Beyond Use Date: 10/4/26
Lot / date codesLot#: LG342009076, Beyond Use Date: 10/4/26

These are the identifiers FDA published for this recall. Most recall notices list no UPC or model number at all — if the code on your item is not shown here, that does not mean the item is excluded. Check the official notice, or contact the company.

This is an automatically maintained record of an official recall notice. Details can change; always follow the official notice linked above. See all records in the Recall Database.