Astral SteriTech recalls Ampicillin 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 Ampicillin for Injection, USP 10g per pharmacy bulk package because it may not be sterile. This could lead to infections if used improperly. The recall affects all lots within the expiry date.
The product may not be sterile, which can cause serious infections if injected. This is a critical issue for medical use as infections can lead to severe complications or death.
Healthcare professionals and pharmacies that use this product for medical injections. Patients receiving this medication under a prescription are at risk if the product is not sterile.
Check for the product name 'Ampicillin for Injection, USP 10 g per Pharmacy Bulk Package' with NDC 66794-224-15. All lots within the expiry date are affected.
Identify the product by its name and NDC code 66794-224-15 to confirm it is part of this recall.
The recall states there is a lack of assurance of sterility, so it is not safe to use as it may cause infections.
The recall record does not specify replacement options or instructions for returns.
The recall record does not provide specific actions for affected users beyond checking product details.
We’ve drafted a message you can send Astral SteriTech to request your refund or repair — edit it as you like.
Subject: Recall D-0584-2023 — Astral SteriTech Astral SteriTech Hello, I own a Astral SteriTech that is covered by recall D-0584-2023 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.
