Greenwich Rx compounded glutathione injection recalled for elevated endotoxin levels
What this means
Greenwich Rx, a compounding pharmacy, is recalling specific lots of compounded glutathione injection due to potential elevated endotoxin levels. Elevated endotoxins in injectable products can cause serious reactions including fever, low blood pressure, and in severe cases, anaphylactic shock or death. The affected product was distributed nationwide between June 26 and September 21, 2026.
- If you received glutathione from one of the recalled lots (check the lot number on your vial), stop using it immediately.
- Follow the disposal instructions provided in the recall notification you received by mail.
- Contact your healthcare provider if you experienced any health issues after using this product.
- Report any adverse reactions to FDA MedWatch at www.fda.gov/medwatch/report.htm or call 1-800-332-1088.
- Contact Sedgwick at (866) 552-4916 or GreenwichRx7542@sedgwick.com with questions (Monday–Friday, 8 AM–5 PM ET).
Product photos
The agency's original wording
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.
Official notice
https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/greenwich-rx-issues-voluntary-nationwide-recall-compounded-glutathione-due-elevated-endotoxin-levelsWant us to check the next one for you?
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