FDA-Drug2026-10-27Class IPROCESSING DEFECT
Greenwich Rx glutathione vials recalled over microbial contamination
What this means
Greenwich Rx is recalling 4,319 vials of its 200 mg/mL glutathione injection (10 mL multi-dose vials, for subcutaneous use only) because they may be contaminated with microbes. The recall covers 12 lots with beyond-use dates from October 2 to November 26, 2026, distributed nationwide. No injuries have been reported.
- Check the vial label for Greenwich Rx glutathione and compare the lot number and BUD date with those listed in the recall.
- Stop using any affected vials and contact your prescriber or pharmacy about replacement or safe disposal.
- The notice does not specify a remedy, so contact Greenwich Rx directly for guidance on refunds or returns.
The agency's original wording
Hazard
Microbial Contamination of Sterile Products
Intended for
Adults
Illnesses reported
None reported
Sold states
US Nationwide in th USA
Affected count
4,319 vials
Manufactured in
9733 Fm 2902 Rd. Suite 100, Tomball, Texas, United States
Products
Glutathione Injection (Glutathione-L, Ascorbic Acid, Sodium Hydroxide, Bacteriostatic Water), 200 mg/mL, 10 mL multi-dose vial, Rx only, Subcutaneous Only, Greenwich Rx.
Official notice
https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=D-0084-2027Also reported as
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