Reliance Life Sciences recalls Azacitidine injections due to potential lack of sterility. This could cause infections if used. Patients with prescriptions should check their product details.
Lack of Sterility Assurance
Reliance Life Sciences is recalling Azacitidine injections because they may not be sterile. Using these products could lead to infections, especially for patients receiving them through medical treatment.
The injections may not be sterile, which can cause infections if used. This is a risk for patients receiving the medication through medical procedures.
Patients prescribed Azacitidine injections by a doctor are affected. Those using the product without medical supervision are not at risk.
Check for the lot numbers RAZM0425A to RAZM2025A on the vial packaging. The product was manufactured for Somerset Therapeutics in New Jersey and sold with specific expiration dates.
Look for lot numbers RAZM0425A through RAZM2025A on the vial packaging.
The product may not be sterile, which could cause infections. Do not use if you have the recalled lot numbers.
Check the lot numbers on the vial: RAZM0425A to RAZM2025A. The product was manufactured for Somerset Therapeutics in New Jersey.
Check the product details and contact your doctor or the manufacturer if you have the recalled lot numbers.
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-0674-2026 — Reliance Life Sciences Reliance Life Sciences Hello, I own a Reliance Life Sciences that is covered by recall D-0674-2026 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.
