Class II · ModerateActive recall
Pemetrexed for Injection 500mg/Vial
Could cause temporary or reversible harm; serious harm is unlikely.
Does this affect you?
Check your lot numberLot, expiry: RPTH0125A Jan 31, 2028; RPTH0225A Jan 31, 2028; RPTH0325A Jan 31, 2028; RPTH0725A Apr 30, 2028;
Where it was soldNationwide in the USA
Find the lot number printed on your box or bottle. If it matches — and you take this medicine — call your pharmacist. Don't stop a prescribed medicine on your own.
What happened
Lack of Sterility Assurance
What to do
- Check the lot number and expiry on your medicine against the recall above.
- Talk to your pharmacist or doctor before changing anything — don't stop on your own.
- Report any problems to FDA MedWatch (1-800-FDA-1088 or fda.gov/medwatch).
Who makes it
| Distributed by / for | Somerset Therapeutics, LLC., Somerset, NJ 08873 |
| NDC | 70069-0835-01 |
Show the full FDA record
| Full product label | Pemetrexed for Injection 500mg/Vial, 1 50 mL Single-Dose Vial per carton, For intravenous use only, Rx only, Manufactured for: Somerset Therapeutics, LLC., Somerset, NJ 08873 NDC: 70069-0835-01 |
| Recalling firm | Reliance Life Sciences Private Limited |
| Distribution | Nationwide in the USA |
| Quantity | 5,020 vials |
| Recall initiated | 2026-06-24 |
| Report date | 2026-07-15 |
| Recall completed | — |
| Recall number | D-0672-2026 |
| Classification | Class II |
| FDA status | Ongoing |
| Origin on file | Navi Mumbai N/A India |
Source: U.S. FDA enforcement database (openFDA). Look this up on the official FDA recalls site ↗
This is public FDA recall information, not medical advice. A recall does not always mean your specific bottle is affected. Never stop a prescribed medicine without asking your pharmacist or doctor.