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Quick answer: On October 1, 2026, Greenwich Rx, a compounding pharmacy in Tomball, Texas, recalled ten lots of Glutathione Injection 200 mg/mL because of potential elevated endotoxin levels. The vials were dispensed to patients nationwide between June 26 and September 21, 2026. It is the fourth Texas pharmacy to recall injectable glutathione since August. If you became ill after a glutathione shot or IV, call 817-870-2102 for a free, confidential case review.
What Greenwich Rx recalled
The recall covers compounded glutathione 200 mg/mL in 10 mL multidose vials, intended for subcutaneous injection, meaning injection under the skin. Greenwich Rx is recalling the product to the consumer level and is notifying customers by mail.
| Lot number | Beyond-use date |
|---|---|
| 0060-062426-1 | Oct 2, 2026 |
| 0060-062726-1 | Oct 5, 2026 |
| 0060-070926-1 | Oct 17, 2026 |
| 0060-071426-1 | Oct 22, 2026 |
| 0060-071426-2 | Oct 22, 2026 |
| 0060-072026-1 | Oct 28, 2026 |
| 0060-072726-1 | Nov 4, 2026 |
| 0060-072926-1 | Nov 6, 2026 |
| 0060-073126-1 | Nov 8, 2026 |
| 0060-080426-1 | Nov 12, 2026 |
The lot number and beyond-use date are printed on the vial label. You can also check any lot from all four recalls with the glutathione recall lot checker.
Two patients needed emergency care after IV use
Greenwich Rx says it has received two reports involving patients who received emergency department care following intravenous (IV) administration of a glutathione product that was not formulated for IV use. The recall notice does not say who gave those doses or where.
The notice carries the same risk statement as the three earlier recalls: there is a reasonable probability that injectable products with elevated endotoxin levels could cause significant medical events including fevers, hypotension, inflammatory reactions, anaphylactic shock, and death.
The fourth Texas glutathione recall in two months
- August 5, 2026: Victory Medical Center Pharmacy, Austin, three lots.
- August 19, 2026: Optimal Balance Pharmacy, Houston, one lot shipped to 14 states.
- September 11, 2026: Centric Compounding, Houston, six lots of glutathione, Myers’ Cocktail, and Tri-Immune Boost.
- October 1, 2026: Greenwich Rx, Tomball, ten lots.
On August 27, 2026, the FDA said that pharmacies involved in adverse event reports had obtained their glutathione from a single lot supplied by Medisca Inc., and that it was labeled dietary supplement grade. The Greenwich Rx recall does not name the supplier of its glutathione. We explain the FDA notice here: FDA warns compounders about supplement-grade glutathione.
If you received Greenwich Rx glutathione
- Stop using it. Do not take another dose from a recalled lot.
- Photograph the vial label before you do anything else: lot number, beyond-use date, pharmacy name, and your prescription label.
- Talk to a lawyer before you throw the vial away. The recall letter includes disposal instructions, but if you had a reaction, the vial and its label may be the best proof of what you received.
- Get medical care if you are unwell, and tell the doctor exactly what you were given, when, and how.
- Keep the paperwork: the recall letter, shipping box, receipts, and messages with the prescriber or clinic.
Greenwich Rx has directed recall questions to Sedgwick at (866) 552-4916, weekdays 8 a.m. to 5 p.m. Eastern.
If a clinic gave you glutathione by IV
Many patients never see the vial. If you had a glutathione drip or push at a med spa, IV bar, or clinic and became ill, ask the clinic in writing which pharmacy made the product, which lot it came from, and what route the vial was labeled for. Depending on the answers, responsibility may rest with the pharmacy, with the provider who administered the product, or with both.
How we can help
The Law Offices of John David Hart filed suit on August 14, 2026 in Travis County, Texas against Victory Medical Center Pharmacy on behalf of a patient hospitalized after a glutathione infusion, and the firm is reviewing claims from patients of all four recalls, in any state. Read the full guide, including symptoms, deadlines, and every recalled lot: Glutathione Recall Lawsuit.
Call 817-870-2102. The case review is free, and there is no fee unless we win.
Source: Greenwich Rx recall announcement, published by the FDA, October 1, 2026.
This article is general information about a publicly announced product recall and is not legal advice. Contacting the firm does not create an attorney-client relationship. Every case is different, and prior results do not guarantee a similar outcome.
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