Astral SteriTech recalls Ceftriaxone 500mg injections due to potential lack of sterility. This could lead to infections if used. Affected lots are all within expiry dates.
Lack of Assurance of Sterility
Astral Steri: Ceftriaxone 500mg injections are recalled because they may not be sterile. Using these could cause infections, especially in medical settings.
The injections may not be sterile, which can lead to infections if used. This is a risk in medical settings where the product is administered.
Prescription patients using Ceftriaxone 500mg injections for medical treatment. Healthcare providers who administered these injections are at higher risk.
Check for the product name 'Ceftriaxone for Injection, USP 500 mg per vial, Rx only'. All lots within expiry dates are affected.
Look for the NDC 66794-212-42 on the vial label.
The recall states there is a risk of lack of sterility, so it is not safe to use.
Check the NDC number 66794-212-42 on the vial label.
The recall does not specify a remedy, so contact your healthcare provider for guidance.
We’ve drafted a message you can send Astral SteriTech to request your refund or repair — edit it as you like.
Subject: Recall D-0612-2023 — Astral SteriTech Astral SteriTech Hello, I own a Astral SteriTech that is covered by recall D-0612-2023 from Astral SteriTech. 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.
Experiences, tips, and questions from readers. Every comment is reviewed before it appears.
No comments yet — be the first to share your experience.
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.
