Astral SteriTech recalls Ceftriaxone injection (10g bulk) due to lack of sterility assurance. All lots within expiry date are affected. Contact for return instructions.
Lack of Assurance of Sterility
Astral SteriTech is recalling Ceftriaxone injection (10g bulk) because it may not be sterile. This could lead to infections if used improperly. Patients should not use this product until the recall is resolved.
The product lacks assurance of sterility, meaning it could contain harmful bacteria or contaminants. If injected, this could cause serious infections or other health issues. The risk is particularly concerning for medical procedures where sterility is critical.
Prescription drug users who received this specific Ceftriaxone injection from the manufacturer. Healthcare providers and patients using the product are at risk if the injection is not sterile.
Check for the product name 'Ceftriaxone for Injection, USP 10 grams per Pharmacy Bulk Package' with NDC 70594-098-01. All lots within the expiry date are affected.
Do not use the recalled Ceftriaxone injection product until the recall is resolved.
The product may not be sterile, so it is not safe to use. Astral SteriTech has recalled it due to lack of sterility assurance.
Check for the product name 'Ceftriaxone for Injection, USP 10 grams per Pharmacy Bulk Package' with NDC 70594-098-01. All lots within the expiry date are affected.
Stop using it immediately and contact Astral SteriTech for return instructions.
We’ve drafted a message you can send Astral SteriTech to request your refund or repair — edit it as you like.
Subject: Recall D-0620-2023 — Astral SteriTech Astral SteriTech Hello, I own a Astral SteriTech that is covered by recall D-0620-2023 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.
