Class II
FDA
Greenwich Rx Compounded Glutathione recalled over See official notice
Greenwich Rx Compounded Glutathione was recalled on October 1, 2026 because of see official notice. It is a Class II recall (possible temporary or reversible harm). Affected area: nationwide. Do not eat this product. Check the official FDA notice for affected lot codes and instructions.
HazardSee official notice
Risk levelClass II
Affected areaNationwide
CategoryFood
What to do
Do not eat this product. Check the official FDA notice for affected lot codes and instructions.
Confirm the details against the official FDA notice before acting.
Does this affect you?
Check the product in your home against the recalled item:
- Product as filed
- Greenwich Rx — Voluntary Nationwide Recall of Compounded Glutathione Due to Elevated Endotoxin Levels
The notice lists no UPC or lot code. Match the brand, product name and package size against the official FDA notice.
Full recall details
- Reason for recall
- IMMEDIATE RELEASE - Tomball, Texas – October 1, 2026 – Greenwich Rx, a 503A compounding pharmacy, is voluntarily recalling specific lots of its compounded glutathione to the consumer level. The product is being recalled due to potential elevated endotoxin levels.
- Hazard class
- Class II — possible temporary or reversible harm
- Recalling company
- Greenwich Rx
- Recall type
- Voluntary
- Quantity
- Distribution
- The glutathione was distributed to patients nationwide between June 26, 2026, and September 21, 2026.
Compiled from the official FDA record by our data rules — how we build these pages. Spotted an error? Report it.
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