Amerisource Health Services is recalling Voriconazole 50mg tablets (30 doses per carton) because they were repackaged by a supplier, potentially affecting drug safety.
cGMP Deviations: Received notification from their supplier requesting they perform a recall due to the fact they repackaged the product.
Amerisource Health Services is recalling Voriconazole 50mg tablets due to repackaging by a supplier. This recall is for safety reasons related to manufacturing practices.
The recall is due to repackaging by a supplier, which may have led to contamination or incorrect labeling. This could affect the safety and effectiveness of the medication.
Patients prescribed Voriconazole 50mg tablets by a healthcare provider who received this specific packaging are affected. Those with the recalled lot number (1014138) and expiration date (04/30/2025) are most at risk.
Check for Voriconazole 50mg tablets in cartons with 30 doses (3 blister cards, 10 doses per card). Look for lot number 1014138 and expiration date 04/30/2025.
Verify the lot number and expiration date on the carton to confirm if it matches the recalled batch (lot #1014138, exp 04/30/2025).
The recall is due to repackaging by a supplier, which may have led to contamination or incorrect labeling.
Check the lot number and expiration date on the carton. If it matches the recalled batch (lot #1014138, exp 04/30/2025), contact your healthcare provider.
The official notice does not specify a remedy beyond checking product details and contacting a healthcare provider.
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-0307-2025 — Amerisource Health Services Amerisource Health Services Hello, I own a Amerisource Health Services that is covered by recall D-0307-2025 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.