Reliance Life Sciences recalls Pemetrexed for Injection 500mg/vial due to lack of sterility assurance. This medication is for IV use only with a prescription. Affected lots expire Jan 2028.
Lack of Sterility Assurance
Reliance Life Sciences is recalling Pemetrexed for Injection 500mg/vial because it may not be sterile. This could lead to infections if used improperly. Patients should not use the recalled product without contacting their doctor.
The product may not be sterile, which could cause infections if injected. This is a serious risk for patients receiving intravenous medication.
Patients prescribed Pemetrexed for Injection 500mg/vial by a doctor. Those using the recalled lots (RPTH0125A to RPTH0725A) are most at risk.
Check the vial label for the lot numbers RPTH0125A, RPTH0225A, RPTH0325A, or RPTH0725A. The product expires by January 31, 2028.
Do not use the recalled Pemetrexed injection vials if you have the specified lot numbers.
The official recall states there is a lack of sterility assurance, so it is not safe to use without contacting your doctor.
Affected lots are RPTH0125A, RPTH0225A, RPTH0325A, and RPTH0725A, all expiring January 31, 2028.
Check the vial label for the lot numbers listed above. The product is for intravenous use only with a prescription.
We’ve drafted a message you can send Reliance Life Sciences to request your refund or repair — edit it as you like.
Subject: Recall D-0672-2026 — Reliance Life Sciences Reliance Life Sciences Hello, I own a Reliance Life Sciences that is covered by recall D-0672-2026 from Reliance Life Sciences. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
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The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
