Astral SteriTech recalls Ampicillin injections due to potential lack of sterility. Affected lots may cause infections if used improperly. Contact for return instructions.
Lack of Assurance of Sterility
Astral Steri: Ampicillin injections (1g per vial) are recalled because they may not be sterile. Using these could lead to infections, especially in medical settings.
The product may not be sterile, which can cause infections if injected. This is a serious risk for medical use where contamination could lead to health complications.
Healthcare providers and patients prescribed this medication. Those using the recalled product for medical treatment are at risk.
Check for the product name 'Ampicillin for Injection, USP 1g per vial', Rx only, and the NDC 66794-222-41. All lots within the expiration date are affected.
Identify the product by name, NDC 66794-222-41, and expiration date.
The recall states there is a lack of assurance of sterility, so it is not safe to use.
Look for Ampicillin for Injection, USP 1g per vial, NDC 66794-222-41, and all lots within expiration date.
The recall does not specify a remedy, so contact the manufacturer for 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-0582-2023 — Astral SteriTech Astral SteriTech Hello, I own a Astral SteriTech that is covered by recall D-0582-2023 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.
