Recall Summary
| Recall number | D-0772-2026 |
| Issued by | U.S. Food and Drug Administration |
| Date | 2026-08-19 |
| Company | Victory Medical Center Pharmacy |
| Units affected | 91 |
| Severity | Class I |
Remedy: Follow the instructions in the official notice linked below. The agency record for this recall did not contain remedy text we could verify against this product, so we have not reproduced it here.
Read the official U.S. Food and Drug Administration recall notice
The victory medical recall involves a sterile injectable drug pulled from the market in August 2026. Victory Medical Center Pharmacy recalled Glutathione (MDV) injection, 200 mg/mL, in 30 mL vials. The U.S. Food and Drug Administration assigned it recall number D-0772-2026 on August 19, 2026. The reason is microbial contamination of sterile products. Out-of-specification results were obtained for bacterial endotoxin. The FDA classified it as Class I, the most serious category. That classification matters to anyone who received this product.
What the Victory Medical Recall Covers
The victory medical recall covers one specific compounded sterile injectable. The product is Glutathione (MDV), 200 mg/mL, packaged in a 30 mL vial. Each milliliter contains Glutathione 200 mg and Ascorbic Acid 20 mg. It also contains Benzyl Alcohol 1.5% and Sodium Hydroxide as a pH adjuster. The base is sterile water for injection. The product carries the VMC designation on its labeling.
The recalling firm is Victory Medical Center Pharmacy. The scope of the victory medical recall is 91 units. That is a small quantity by pharmaceutical standards. However, a small unit count does not mean small risk. Compounded sterile injectables often go directly into patients at clinics. As a result, a limited batch can still reach many people quickly.
The FDA record does not list broad retail distribution for this product. Compounded drugs like this typically move through clinics, medical offices, and direct patient administration. For example, glutathione injections are often given in wellness and infusion settings. Consumers rarely buy them off a store shelf. In most cases, the provider who administered the injection holds the lot records.
If you are trying to identify the product, look for the full description. The strength, the 30 mL multi-dose vial format, and the VMC marking are the key identifiers. Your clinic or pharmacy should be able to confirm whether the vial used on you falls within the victory medical recall. Ask them directly and ask for it in writing.
The Hazard and Reported Injuries
The stated hazard is microbial contamination of sterile products. Specifically, out-of-specification results were obtained for bacterial endotoxin. Endotoxins are substances released from certain bacteria. They can be present even when no live bacteria remain. Standard sterilization does not always remove them. That is why endotoxin testing is a separate requirement for injectables.
Endotoxin in an injectable product is treated seriously by regulators. When injected, endotoxins can trigger a strong inflammatory response in the body. Reported effects in medical literature include fever, chills, and shaking. More severe reactions can involve blood pressure changes and organ stress. The risk generally rises with the dose delivered and the patient’s underlying health.
Whether any injuries have been reported in connection with this specific recall is not stated in the agency record. This guide does not claim that anyone was harmed. It also does not claim that no one was harmed. The record is simply silent on that point. Readers should not read the Class I designation as proof of injury. Class I reflects the potential for serious harm, not a confirmed count of it.
| Recall number | D-0772-2026 |
|---|---|
| Issuing agency | U.S. Food and Drug Administration |
| Recall date | August 19, 2026 |
| Company | Victory Medical Center Pharmacy |
| Product | Glutathione (MDV), 200 mg/mL, 30 mL vial |
| Units affected | 91 units |
| Hazard | Microbial contamination — out-of-specification bacterial endotoxin results |
| Severity classification | Class I |
Class I is the FDA’s highest severity tier. It is used when there is a reasonable probability that exposure will cause serious adverse health consequences or death. It is not used lightly. For example, the FDA reserves Class I for contaminated injectables, undeclared major allergens, and similar hazards. The victory medical recall carries that top-tier designation.
What To Do If You Own This Product
Stop using the product immediately if you have it in your possession. Do not administer it. Do not let anyone else administer it. This applies to clinics, medical offices, and any individual holding vials. Set the product aside and label it so it is not used by mistake.
Next, confirm identification. Match the product description against what you have on hand. Check the drug name, the 200 mg/mL strength, and the 30 mL vial size. Look for the VMC marking. If you received an injection rather than holding a vial, contact the clinic that treated you. Ask them to check their records against recall D-0772-2026.
For return, refund, or replacement instructions, follow the official notice. The remedy details for this recall are set out by the FDA and the recalling firm, not by this page. Read them directly here: FDA Enforcement Report — official recall notice. Do the exact steps that notice describes. Typically, notices explain how to quarantine product and who to contact.
If you received this injection and feel unwell, contact a healthcare provider. Do not wait to see if symptoms pass on their own. Fever, chills, or a sudden feeling of illness after an injection deserve prompt evaluation. As a result of the endotoxin finding, providers may want to know the timing of your dose. Keep your receipts, appointment records, and any product packaging.
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Does a Victory Medical Recall Mean You Can Sue?
A recall is a safety action. It is not a lawsuit. The victory medical recall is a regulatory step to remove a product from use. It does not create a legal claim by itself. It does not mean money is available to anyone. Many recalls end with returns and corrections and nothing more.
A legal claim generally requires more than a recall notice. In most cases, a person needs an actual injury. They also need a link between that injury and the recalled product. Lawyers call that link causation. Medical records, dosing dates, and lot documentation often matter. Without those pieces, a claim is difficult regardless of how serious the recall sounds.
This guide does not report any lawsuit over the victory medical recall. No litigation connected to recall D-0772-2026 has been verified here. Do not assume one exists. However, that can change over time, and the absence of a case today says nothing about tomorrow.
If you believe you were harmed, speak with a licensed attorney in your state. A consultation is typically free. An attorney can review your records and tell you whether you may be eligible to pursue a claim. Nothing on this page is legal advice, and no outcome is guaranteed. Deadlines called statutes of limitations apply, so do not delay.
How Recalls Connect to Mass Tort Cases
Recalls sometimes become evidence in later litigation. A recall notice can help establish what a company knew and when. Internal testing records behind a recall can become discovery material. For example, an out-of-specification test result shows the product failed a required standard. That kind of documentation is often central to product liability claims.
History offers clear examples. The Philips CPAP recall of 2021 involved foam degradation in breathing devices. It later became the basis of consolidated federal litigation. The Takata airbag recalls involved inflators that could rupture. Those recalls also preceded extensive litigation and a corporate bankruptcy. In both cases, however, the recall was the starting point, not the verdict. Individual plaintiffs still had to prove injury and causation on their own facts.
Frequently Asked Questions
What product is covered by the victory medical recall?
The recall covers Glutathione (MDV) injection, 200 mg/mL, in 30 mL vials from Victory Medical Center Pharmacy. Each mL contains glutathione 200 mg, ascorbic acid 20 mg, benzyl alcohol 1.5%, and sodium hydroxide in sterile water. The FDA recall number is D-0772-2026.
Why was the product recalled?
Testing produced out-of-specification results for bacterial endotoxin, which the FDA describes as microbial contamination of sterile products. Endotoxin in an injectable can trigger serious inflammatory reactions. The FDA classified the victory medical recall as Class I, its most serious tier.
Were any injuries reported?
The agency record does not state whether injuries were reported. This page will not claim harm occurred or that it did not. If you received this injection and feel unwell, contact a healthcare provider promptly.
Were You Injured by a Recalled Product?
A recall by itself is a safety action, not a legal claim. However, if a recalled product caused a real injury, you may be eligible to pursue compensation. A licensed attorney can review your situation at no upfront cost — most work on contingency, meaning you pay nothing unless you recover.
Official Sources & Resources
Verify every recall against the issuing agency before acting:
- U.S. Food and Drug Administration: official recall database — the record of truth for this notice
- CPSC: cpsc.gov — household goods, toys, furniture, appliances
- FDA: fda.gov — food, drugs, and medical devices
- NHTSA: nhtsa.gov — vehicles, tires, and child car seats
- USDA FSIS: fsis.usda.gov — meat, poultry, and egg products
Content last reviewed August 2026. This is general educational information, not legal advice. If you notice outdated information, please contact us.
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Attorney Advertising. The information on this page is provided for general informational purposes only and does not constitute legal advice. A product recall is a safety action by a manufacturer or regulator and does not by itself establish liability or create a legal claim. No attorney-client relationship is created by accessing or using this content. Every case is unique. If you believe you were harmed by a recalled product, consult a licensed attorney in your jurisdiction.