FDA Drug recall · Reported August 19, 2026
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.
Microbial Contamination of Sterile Products - out of specifications results were obtained for bacterial endotoxin.
Victory Medical Center Pharmacy recalled Glutathione (MDV), 200 mg/mL, 30 mL vial, each mL contains Glutathione 200 mg, Ascorbic A… - a critical-severity action.
Glutathione (MDV), 200 mg/mL, 30 mL vial, each mL contains Glutathione 200 mg, Ascorbic A… was recalled by Victory Medical Center Pharmacy in August 19, 2026. Reason: Microbial Contamination of Sterile Products - out of specifications results were obtained for bacterial endot…. Check the official notice for the remedy. Verify recall #D-0772-2026 with the FDA Drug before acting.
The recall
Victory Medical Center Pharmacy issued this critical-severity FDA Drug recall-Microbial Contamination of Sterile Products - out of specifications results were obtained for bacterial endot….
- Critical
- severity level
- 91 units
- affected scope
- Class I
- classification
- August 19, 2026
- reported
Sourced from official FDA Drug enforcement records. Verify recall #D-0772-2026 with the agency before acting. Full product description, hazard, remedy, and related recalls are below.
Recall Insight
This FDA Drug action (record #D-0772-2026) was formally reported on August 19, 2026, with the manufacturer initiating the action on July 1, 2026. It is classified under Critical severity (Class I), with a current status of Ongoing. Victory Medical Center Pharmacy is listed as the recalling firm, operating out of Austin, TX. Federal records list the affected scope as 91.
The documented reason for this recall is: Microbial Contamination of Sterile Products - out of specifications results were obtained for bacterial endotoxin. Distribution data in the federal record shows the product reached: USA Nationwide. Distribution scope directly affects the consumer exposure window and determines whether a recall remains regional or escalates into a nationwide advisory.
Within the same product category the archive holds 6 closely related recalls, 6 from FDA Drug - clustering in a narrow category often points to a systemic quality-control or supplier issue rather than a one-off defect. Always verify the recall number against the official agency record before acting.
Drugs & Medications recalls over time
Where this recall sits in its category - 14,472 drugs & medications recalls on record
Of 88,244 recalls with an agency hazard classification, 19,068 are high severity, 64,652 moderate, and 4,524 low. A further 16,179 CPSC/NHTSA recalls have no agency class and are excluded from this split. This recall is classified high severity.
Counts reflect market size and reporting activity, not inherent danger, we do not rank products by risk from raw recall volume.
Product description
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.
Reason for recall
Microbial Contamination of Sterile Products - out of specifications results were obtained for bacterial endotoxin.
Recall Profile
| Attribute | Value |
|---|---|
| Agency | U.S. Food and Drug Administration |
| Severity class | Critical (Class I) |
| Status | Ongoing |
| Recall number | D-0772-2026 |
| Date reported | August 19, 2026 |
| Date initiated | July 1, 2026 |
| Recalling firm | Victory Medical Center Pharmacy |
| Firm location | Austin, TX |
| Affected scope | 91 |
| Distribution | USA Nationwide |
Profile values are sourced directly from the official FDA Drug enforcement record. Source: U.S. Food and Drug Administration.
What to do with this recall
Match your product against the recall record, then act on the agency remedy.
- Check the recall number (D-0772-2026) and product description against the item you own. Search the archive
- Confirm the current status with FDA Drug before acting, recall details can be updated.
- This is a Class I (high-risk) recall, stop using the product immediately and follow the disposal or return instructions. What to do next
This page summarizes the official FDA Drug record for research and awareness; it is not legal, medical, or safety advice. Verify with the issuing agency before acting.
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Nationwide recalls with similar severity or category timing
Drug and device notices outside this firm and state, matched by severity timing and product category.
Similar severity · nearest report date
Same archive severity grade (Critical), closest by report date among other firms and states.
Similar Drugs & Medications · nearest report date
Same product category, closest by report date among other firms and states (deduped against the severity set).
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Methodology · Corrections · Archive as of August 2026