Could cause temporary or reversible harm; serious harm is unlikely.
Discolored solution. The firm has received market complaints reporting green to dark green discoloration in certain vials
| Brand name | PEMRYDI RTU |
| Generic name | PEMETREXED DISODIUM |
| Active ingredient(s) | PEMETREXED DISODIUM HEMIPENTAHYDRATE |
| Distributed by / for | Amneal Pharmaceuticals LC, Bridgewater, NY 08807 |
| NDC | 70121-2453-1 |
| Full product label | PEMRYDI RTU (pemetrexed injection), 100 mg/10 mL (10 mg/mL), Single-dose vial, Rx only, Manufactured by: Zydus Lifesciences Limited, Ahmedabad, India; Distributed by: Amneal Pharmaceuticals LC, Bridgewater, NY 08807. NDC: 70121-2453-1 |
| Recalling firm | Shilpa Medicare Limited |
| Distribution | Nationwide in the USA. |
| Quantity | 18,434 10mL vials |
| Recall initiated | 2026-07-29 |
| Report date | 2026-08-26 |
| Recall completed | — |
| Recall number | D-0764-2026 |
| Classification | Class II |
| FDA status | Ongoing |
| Origin on file | Jadcherla, Mahabubnagar District India |
Source: U.S. FDA enforcement database (openFDA). Look this up on the official FDA recalls site ↗