Amerisource Health Services recalls Rifampin Capsules USP 300mg due to failed impurities and degradations. This medication is prescription-only and may pose health risks if used.
Failed Impurities/Degradations Specifications
Amerisource Health Services is recalling Rifampin Capsules USP 300 mg (100 capsules per carton) because they failed impurities and degradations specifications. This could pose health risks if the medication is used as intended.
The capsules failed impurities and degradations specifications, which means they may contain harmful substances or break down in a way that affects safety. This could lead to health risks if the medication is taken as directed.
Prescription patients who have the specific lot number (1007805) of Rifampin Capsules USP 300 mg. Those using this medication for conditions like tuberculosis are most at risk.
Check for the carton NDC 60687-586-01 (Individual Dose NDC: 60687-586-11) with lot number 1007805. The capsules are prescription-only and expire December 31, 2023.
Look for the carton NDC 60687-586-01 with lot number 1007805 on the packaging.
The recall indicates the capsules failed impurities and degradations specifications, so they may not be safe to use. Consult your healthcare provider for advice.
The recall does not specify a remedy, so contact Amerisource Health Services for guidance on next steps.
Check the carton NDC 60687-586-01 with lot number 1007805. The capsules are prescription-only and expire December 31, 2023.
We’ve drafted a message you can send Amerisource Health Services to request your refund or repair — edit it as you like.
Subject: Recall D-0165-2023 — Amerisource Health Services Amerisource Health Services Hello, I own a Amerisource Health Services that is covered by recall D-0165-2023 from Amerisource Health Services. 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.
