Astral SteriTech recalls Ceftriaxone 2g vials due to lack of sterility assurance. This injectable antibiotic poses a risk of infection if used improperly. Affected products include all lots within expiry date.
Lack of Assurance of Sterility
Astral SteriTech has recalled Ceftriaxone for Injection, 2 grams per vial, because it may not be sterile. This could lead to infections if the medication is used. The recall affects all vials within their expiration date.
The medication may not be sterile, which could cause infections in patients after injection. This is a serious risk for individuals who must receive the antibiotic treatment.
Prescription patients who received this specific antibiotic vial from the manufacturer. Healthcare providers using the product for medical treatments are at higher risk.
Check for the product name 'Ceftriaxone for Injection, USP, 2 grams per vial' on the label. The manufacturer is Astral SteriTech Private Ltd. and it was sold with NDC 70594-097-02. All lots within the expiration date are affected.
Look for the product name 'Ceftriaxone for Injection, USP, 2 grams per vial' and NDC 70594-097-02 on the label.
The recall states there is a lack of assurance of sterility, so it is not safe to use as it could cause infections.
Check for the product name 'Ceftriaxone for Injection, USP, 2 grams per vial' with NDC 70594-097-02 on the 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-0619-2023 — Astral SteriTech Astral SteriTech Hello, I own a Astral SteriTech that is covered by recall D-0619-2023 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.
