Reliance Life Sciences recalls Pemetrexed for Injection 100mg/vial due to lack of sterility assurance. This drug, used for intravenous treatment under prescription, may pose infection risks if improperly handled.
Lack of Sterility Assurance
Reliance Life Sciences is recalling Pemetrexed for Injection 100mg/vial products because they lack sterility assurance. This means the medication could cause infections if used improperly. Patients should not use these products without contacting their healthcare provider.
The medication lacks sterility assurance, meaning it may contain contaminants that could cause infections when administered intravenously. This risk is particularly concerning for patients receiving cancer treatments who require precise medication handling.
Patients prescribed Pemetrexed for Injection 100mg/vial by a healthcare provider. Those using the medication for cancer treatment are most at risk due to the potential infection hazard.
Check for the product name 'Pemetrexed for Injection 100mg/Vial' with the lot numbers RPTL0325A, RPTL0425A, RPTL0624B, or RPTL0625A. The product was manufactured by Somerset Therapeutics, LLC in New Jersey.
Patients should contact their healthcare provider to discuss alternative treatment options or whether they need to stop using the recalled medication.
The recall states there is a lack of sterility assurance, so the medication may pose infection risks. Patients should not use it without consulting their healthcare provider.
The affected lot numbers are RPTL0325A, RPTL0425A, RPTL0624B, and RPTL0625A.
Check the product label for the lot numbers mentioned above. The product was manufactured by Somerset Therapeutics, LLC in New Jersey.
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-0671-2026 — Reliance Life Sciences Reliance Life Sciences Hello, I own a Reliance Life Sciences that is covered by recall D-0671-2026 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.
