Glutathione Recall: Greenwich Rx Glutathione Injection 200 mg/mL
Announced 2026-10-28 · FDA
FDA recall of Greenwich Rx Glutathione Injection due to microbial contamination of sterile products. 4,319 vials were distributed nationwide in the United States. The lots have BUD dates from 10/02/2026 to 11/26/2026.
| Brand | Greenwich Rx |
|---|---|
| Product | Glutathione Injection (Glutathione-L, Ascorbic Acid, Sodium Hydroxide, Bacteriostatic Water), 200 mg/mL, 10 mL multi-dose vial, Rx only, Subcutaneous Only, Greenwich Rx. |
| Reason | Microbial Contamination of Sterile Products |
| Severity | critical |
| Units affected | 4319 |
| Distribution | US Nationwide in th USA |
| Agency | FDA |
WHAT YOU SHOULD DO
- Do not use any Greenwich Rx Glutathione Injection from the affected lots.
- Check your vial's lot number against the recall list and discard or return any matching vials.
- Contact Greenwich Rx or your healthcare provider for return, disposal instructions, and possible replacement.
- If you have concerns or experience symptoms, consult your clinician and report adverse events to FDA MedWatch.
How to identify the recalled item
| Lot / date codes | Lot # 0060-062426-1, BUD: 10/02/2026; Lot # 0060-062726-1, BUD: 10/05/2026; Lot # 0060-070926-1, BUD: 10/17/2026; Lot # 0060-071426-1, BUD: 10/22/2026; Lot #0060-071426-2, BUD: 10/22/2026; Lot # 0060-072026-1, BUD: 10/28/2026; Lot # 0060-072726-1, BUD: 11/04/2026; Lot #0060-072926-1, BUD: 11/06/2026; Lot # 0060-073126-1; BUD: 11/08/2026; Lot # 0060-080426-1, BUD: 11/12/2026; Lot #: 0060-080526-1, BUD: 11/13/2026; Lot # 0060-081826-1, BUD: 11/26/2026. |
|---|---|
| Lot / date codes | Lot # 0060-062426-1, BUD: 10/02/2026; Lot # 0060-062726-1, BUD: 10/05/2026; Lot # 0060-070926-1, BUD: 10/17/2026; Lot # 0060-071426-1, BUD: 10/22/2026; Lot #0060-071426-2, BUD: 10/22/2026; Lot # 0060-072026-1, BUD: 10/28/2026; Lot # 0060-072726-1, BUD: 11/04/2026; Lot #0060-072926-1, BUD: 11/06/2026; Lot # 0060-073126-1; BUD: 11/08/2026; Lot # 0060-080426-1, BUD: 11/12/2026; Lot #: 0060-080526-1, BUD: 11/13/2026; Lot # 0060-081826-1, BUD: 11/26/2026. |
These are the identifiers FDA published for this recall. Most recall notices list no UPC or model number at all — if the code on your item is not shown here, that does not mean the item is excluded. Check the official notice, or contact the company.
Other glutathione recalls
This is an automatically maintained record of an official recall notice. Details can change; always follow the official notice linked above. See all records in the Recall Database.