Astral SteriTech recalls bulk ampicillin and sulbactam injection packages due to potential lack of sterility. This affects pharmacy bulk packages with NDC 70594-083-01. No remedy specified in official notice.
Lack of Assurance of Sterility
Astral SteriTech is recalling bulk ampicillin and sulbactam injection packages (NDC 70594-083-01) because they may not be sterile. This could lead to infections if used in medical treatments.
The injections may not be sterile, which can cause infections in patients during medical treatments. This is a serious risk for people receiving injections through these packages.
Pharmacists and healthcare facilities that use these bulk packages for prescriptions. Patients receiving injections from these packages are at risk of infection.
Check for the NDC code 70594-083-01 on the package. These are bulk packages sold for pharmacy use only, not for individual patients.
Look for the NDC code 70594-083-01 on the package label to confirm it's affected.
The official recall notice states there is a risk of lack of sterility, so it is not safe to use without checking the recall status.
The official notice does not specify any remedy or replacement options.
The official notice does not provide specific instructions for affected users.
We’ve drafted a message you can send Astral SteriTech to request your refund or repair — edit it as you like.
Subject: Recall D-0603-2023 — Astral SteriTech Astral SteriTech Hello, I own a Astral SteriTech that is covered by recall D-0603-2023 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.
