VMC: Compounded Glutathione 200 mg/mL Multi-Dose Vials — FDA announcement Aug 5, 2026

Published notice; closure not supplied

A company announcement posted by FDA. The listing date can differ from the original announcement date. The absence of a termination marker does not prove the recall is currently ongoing.

Source date Aug 5, 2026. Retrieved Oct 1, 2026. Last updated Oct 1, 2026.

Archive changed Oct 1, 2026. USDA FSIS records are unavailable; check FSIS directly. Source coverage and dates.

What the record says

Product
Compounded Glutathione 200 mg/mL Multi-Dose Vials
Reason
Elevated Endotoxin level
Classification
Not supplied
Recalling firm
Victory Medical Center Pharmacy
Quantity
Not supplied
Agency-reported status
Company recall announcement
Source record identifier
000db0f5812a862b

Open the official record

Lot and product identifiers

Label fieldDetails supplied by the agency
Lot, code or applicabilityPatients who have product from an affected lot should:; Product | Dosage Form | Lot Number | Expiration Date; VMC Compounded Glutathione 200 mg/mL | Multi-Dose Vial | 1980571 | August 27, 2026; 1981940; 1984345

Match all identifying details in the current notice. A brand name alone is not enough.

Product tables from the announcement

These identifying details come from the company announcement posted by FDA. Check the current notice for revisions.

FDA company announcement, table 1
Product Dosage Form Lot Number Expiration Date
VMC Compounded Glutathione 200 mg/mL Multi-Dose Vial 1980571 August 27, 2026
1981940
1984345

Announcement retrieved Oct 1, 2026. Official announcement.

Distribution

Not supplied

No US distribution state could be established from this record. Check the official notice.

Dates in the source

Fda listing date
Aug 5, 2026
Company announcement date
Aug 5, 2026

FDA company pages use the listing date; enforcement records use initiation dates; CPSC uses recall date; NHTSA uses report-received date. These dates are not interchangeable.

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