Astral SteriTech recalls Cefepime injection vials due to potential lack of sterility. All lots within expiry date are affected. Consumers should contact the manufacturer for details.
Lack of Assurance of Sterility
Astral SteriTech has recalled Cefepime injection vials (1 gram per vial) because they may not be sterile. This could lead to infections if used improperly. The recall covers all lots within the expiry date.
The product may not be sterile, which can cause infections if injected. This risk is serious but the exact mechanism isn't clearly described in the recall notice.
Patients receiving Cefepime injections are affected. Healthcare providers using the product are at risk of administering non-sterile medication.
Check for the product name 'Cefepime for Injection, USP 1 gram per vial'. The NDC code 70594-089-02 and all lots within expiry date are affected.
Reach out to Astral SteriTech for specific instructions on handling the recalled product.
The recall states there is a risk of lack of sterility, so it is not safe to use without contacting the manufacturer first.
Contact Astral SteriTech for specific instructions on handling the recalled product.
Check for the NDC code 70594-089-02 and all lots within expiry date on the product label.
We’ve drafted a message you can send Astral SteriTech to request your refund or repair — edit it as you like.
Subject: Recall D-0609-2023 — Astral SteriTech Astral SteriTech Hello, I own a Astral SteriTech that is covered by recall D-0609-2023 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.
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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.
