Aug 5, 2026FDAactive

Victory Medical Center Pharmacy Issues Voluntary Nationwide Recall of Certain Lots of Compounded Glutathione 200 mg/mL Multi-Dose Vials Due to Elevated Endotoxin Levels

Victory Medical Center Pharmacy

Company announcement

FOR IMMEDIATE RELEASE – August 5, 2026 – Austin, Texas, Victory Medical Center Pharmacy is voluntarily recalling certain lots of Compounded Glutathione 200 mg/mL Multi-Dose Vials to the patient level. The product is being recalled because pharmacy testing identified elevated bacterial endotoxin levels

Risk Statement: There is reasonable probability that injectable products with elevated endotoxin levels could cause significant medical events including fevers, hypotension, inflammatory reactions, anaphylactic shock and death. To date, Victory Medical Center Pharmacy has received reports of adverse events including fever, chills, severe headache, nausea, vomiting, tachycardia, changes in blood pressure, body aches, and instances of injection site reactions.

The affected product information is as follows:

ProductDosage FormLot NumberExpiration Date
VMC Compounded Glutathione 200 mg/mLMulti-Dose Vial1980571August 27, 2026
1981940
1984345

This compounded glutathione was distributed to consumers in Texas, Florida, and New York

Victory Medical Center Pharmacy is notifying its prescribers and patients by telephone and mail and is arranging for retrieval and proper disposition of the recalled product.

Patients who have product from an affected lot should:

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.

Your assistance is appreciated and necessary to prevent consumer illness or patient harm.

Adverse reactions or quality problems experienced with the use of this product may be reported to the FDA's MedWatch Adverse Event Reporting program either online, by regular mail or by fax.

Product images

Official record — FDA enforcement

Official FDA enforcement data — classification, lot codes, and quantities — is published once FDA processes this recall, typically several weeks after the announcement. This page updates automatically when it arrives.

Source: U.S. Food & Drug AdministrationOriginal announcement ↗