Glutathione Injection (Glutathione-L Recall: What To Do

Greenwich Rx recall D-0084-2027 involves an injectable glutathione product sold in multi-dose vials. The U.S. Food and Drug Administration posted the recall on October 28, 2026. The company named in the agency record is Greenwich Rx. The listed hazard is microbial contamination of sterile products. FDA classified the action as Class I, its most serious category. If you use injectable glutathione, this notice matters to you. A contaminated injection can carry germs directly into the body.

What the Greenwich Rx Recall Covers

The recalled product is Glutathione Injection, 200 mg/mL. It comes in a 10 mL multi-dose vial. The label lists Glutathione-L, ascorbic acid, sodium hydroxide, and bacteriostatic water. The vial is marked “Rx only” and “Subcutaneous Only.” The company name on the label is Greenwich Rx.

According to the agency record, the recall covers 4,319 units. That is a large quantity for a single injectable product. However, this page does not list specific lot numbers or expiration dates. As a result, you should check the official FDA notice for lot details. Do not assume your vial is safe just because a lot code is not listed here.

People typically use glutathione injections for wellness, skin, or antioxidant purposes. Because the label says “Rx only,” the product requires a prescription. Some patients inject at home. Others receive the injection at a clinic, med spa, or wellness office. As a result, a vial may sit in a home refrigerator or in a provider’s supply cabinet.

The Greenwich Rx recall applies to the product as described in the FDA record. For example, the strength, vial size, and route of use all help identify it. If your vial matches this description, treat it as possibly affected until you confirm otherwise. Your pharmacist or prescriber can help you compare labels.

The Hazard and Reported Injuries

The listed hazard is microbial contamination of sterile products. Injectable drugs must be sterile. That means they should contain no living bacteria, fungi, or other microorganisms. When sterility fails, an injection can carry germs past the skin’s natural barrier. As a result, even a small dose can cause an infection.

Harm from a contaminated injection can range from mild to severe. For example, a person may get redness, swelling, or pain at the injection site. An abscess can form under the skin. In more serious cases, an infection can spread into the bloodstream. Bloodstream infections can be life-threatening, especially for people with weak immune systems.

Multi-dose vials add another layer of concern. A single vial is punctured many times over days or weeks. If the contents were contaminated from the start, every dose drawn may carry the same risk. Preservatives such as those in bacteriostatic water typically slow bacterial growth. However, they do not make a contaminated product safe.

The FDA record does not say whether any injuries have been reported in connection with this Greenwich Rx recall. We make no claim either way. A Class I designation means FDA found a reasonable probability of serious health consequences or death. It does not, on its own, confirm that anyone has been harmed. The table below summarizes the key facts.

What To Do If You Own This Product

First, stop using the product. Do not inject any more doses from a vial that matches this description. Store the vial somewhere safe, away from children. Do not throw it away yet. You may need it later to confirm the lot number or to document your use.

Next, identify the product. Check the label for “Glutathione Injection,” “200 mg/mL,” and “10 mL multi-dose vial.” Look for “Greenwich Rx” and “Subcutaneous Only.” Then write down any lot number and expiration date on the vial or box. Clear photos of the label are also a good idea.

For the remedy, follow the instructions in the official FDA notice linked on this page. We do not describe the remedy here. The agency record contains remedy text that does not match this product, so we withheld it. The official notice is the safest guide for what to do next. You can search the database here:

FDA Enforcement Report – Drug Recalls

Then talk to a health professional. Contact your prescriber or pharmacist if you used this product recently. Get medical care right away if you notice fever, chills, spreading redness, or warmth at the injection site. In most cases, treating an infection early leads to better outcomes. You can also report side effects through FDA MedWatch.

Keep a written record of each step you take. Note the dates you used the product and any symptoms. Save pharmacy receipts and prescription records. This record will help your doctor. It may also help if you later speak with a lawyer about the Greenwich Rx recall.

Does a Greenwich Rx Recall Mean You Can Sue?

A recall is not a lawsuit. It is a safety action. The Greenwich Rx recall is meant to take a possibly unsafe product out of use. It does not mean a court has found anyone at fault. It also does not create a legal claim on its own.

In most cases, a product liability claim needs more than a recall. Typically, a person must show an actual injury. They must also show the product likely caused that injury. For example, a documented infection that a doctor links to a contaminated injection may support a claim. Medical records, lot numbers, and purchase records often matter a great deal.

As of this writing, we are not aware of any lawsuit filed over this recall. That could change over time. However, you should not assume a case exists or will exist. If you were hurt after using this product, consider speaking with a licensed attorney. Many product liability lawyers offer free consultations.

An attorney can review your facts and explain your options. You may be eligible to pursue a claim, depending on your injury and evidence. No outcome is guaranteed. Deadlines called statutes of limitations also apply. As a result, waiting too long can limit your options, even if your case is strong.

How Recalls Connect to Mass Tort Cases

Recalls often become important evidence in later litigation. A recall notice can show when a company or regulator identified a problem. Internal records and inspection reports may follow. For example, Philips recalled certain CPAP and BiPAP machines in 2021 over degrading sound-abatement foam. Consolidated federal litigation over alleged injuries and economic losses followed that recall.

Takata airbags are another example. Defective inflators led to one of the largest auto recalls in U.S. history. Lawsuits and government actions followed. The 2012 New England Compounding Center outbreak is closer to this topic. Contaminated steroid injections caused fungal meningitis infections and deaths. Lawsuits and criminal convictions followed. However, every case is different.

The Greenwich Rx recall may or may not follow that path. In most cases, mass torts form only when many people report similar injuries. Courts may then group the cases to handle them more efficiently. Until that happens, the best steps are simple. Protect your health, keep your records, and watch for official updates.

Frequently Asked Questions

What product is included in the Greenwich Rx recall?

The recall covers Glutathione Injection, 200 mg/mL, in a 10 mL multi-dose vial labeled “Subcutaneous Only.” The FDA record lists 4,319 units. Check the official notice for lot details.

How serious is the Greenwich Rx recall?

FDA classified it as Class I, its most serious recall category. That means FDA found a reasonable probability of serious health consequences or death. The record does not say whether any injuries have been reported.

Can I file a claim because of the Greenwich Rx recall?

A recall alone is not a claim. If you were injured and the product likely caused it, you may be eligible to pursue one. A licensed attorney can review your situation.

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 November 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.