Fresh Recalls

FDAClass I · Drug · Recall D-0772-2026 · Recalled August 19, 2026

Glutathione (MDV) recall — Victory Medical Center Pharmacy

Agency report date: August 19, 2026.

1. Compare your item

This notice names a product; your particular item is not yet verified. Compare every applicable model, serial, lot, production-date or model-year boundary below.

Product named
Glutathione (MDV)
Company / brand
Victory Medical Center Pharmacy
Lot / serial / date codes
Lot # 1984345, 1980571, 1981940, Use Before Date: 08/27/2026.
Distribution
USA Nationwide
Agency product description and boundaries

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.

Still to verify: match the label on your item with the full official notice, including any exclusions, tables and photos. Some identifiers appear only on the agency website and are absent from this data feed. A missing field does not mean all versions are affected.

If your lot or date falls outside a stated range, this notice has not established that your item is affected. This is not a finding about other recalls or product safety.

2. Agency hazard and consumer action

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

No consumer remedy instructions are supplied in this record. Check the official notice and listed company contact for the agency’s current instructions.

Class I: most serious — reasonable probability of serious health consequences or death.

Affected product: Glutathione (MDV)

3. Open the official notice or contact

Official recall ID
D-0772-2026
Brand
Victory Medical Center Pharmacy
Classification
Class I
Units affected
91
Recall status
Ongoing
Initiated
Voluntary: Firm initiated

Affected products

Companies & origin

Recalling firm location
Austin, TX, United States
Firm address
4303 Victory Dr, 78704-7507

Identifying details (verbatim from the notice)

Product codes / lots
Lot # 1984345, 1980571, 1981940, Use Before Date: 08/27/2026.
Distribution
USA Nationwide
Firm notified the public via
Telephone
FDA event ID
99509
Recall initiated
July 1, 2026
FDA classified
August 19, 2026
FDA report date
August 19, 2026
Verify with the official sources:

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Source: U.S. Food & Drug Administration. Agency excerpts come from the public data feed and may omit tables or later changes; the linked government source is authoritative. Source last checked September 7, 2026 at 6:00 AM UTC. Record retrieved September 7, 2026 at 6:00 AM UTC.

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