Amerisource Health Services recalls Febuxostat 40mg tablets due to CGMP deviations. These prescription drugs may have manufacturing issues affecting safety. Check your NDC numbers for affected lots.
CGMP Deviations
Amerisource Health Services is recalling Febuxostat 40mg tablets (30 tablets per carton) because of manufacturing deviations. This recall affects prescription-only medications that could pose safety risks if the CGMP issues are not resolved.
CGMP deviations refer to manufacturing process failures that could affect product safety and quality. These deviations may result in tablets that don't meet the required standards for safe use, potentially causing health risks. However, the specific nature of the deviations isn't detailed in the recall notice.
Prescription drug users who have Febuxostat 40mg tablets with NDC Carton 60687-538-21 or NDC Unit dose 60687-538-11. Patients with specific lot numbers (1015033 or 1016409) are most at risk.
Check for NDC Carton number 60687-538-21 or NDC Unit dose 60687-538-11 on the packaging. Affected lots are 1015033 (expires 06/30/2025) and 1016409 (expires 08/31/2025).
Look for NDC Carton 60687-538-21 or NDC Unit dose 60687-538-11 on the packaging.
Amerisource Health Services is recalling Febuxostat 40mg tablets due to CGMP deviations in manufacturing.
Check for NDC Carton 60687-538-21 or NDC Unit dose 60687-538-11 with lot numbers 1015033 (expires 06/30/2025) or 1016409 (expires 08/31/2025).
The recall notice does not specify a remedy or action for affected products.
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-0314-2024 — Amerisource Health Services Amerisource Health Services Hello, I own a Amerisource Health Services that is covered by recall D-0314-2024 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.
