Aspen Biopharma recalls voriconazole containers with CGMP deviations. Check lot number HAVZC0020922 (exp. AUG-2026) for affected units.
CGMP Deviations
Aspen Biopharma is recalling voriconazole containers due to CGMP deviations. This means the product may not meet quality standards, though no injuries have been reported.
CGMP deviations indicate potential quality issues in manufacturing. This could affect the medication's safety or effectiveness, though no injuries have been reported.
People who purchased voriconazole containers with lot number HAVZC002:0922 (expiring August 2026) are affected. Patients using this medication are most at risk.
Check for the lot number HAVZC0020922 on the container. The product was packed in a white poly bag containing a black poly bag and shipped in an HDPE container.
Look for lot number HAVZC0020922 on the container.
The recall is for CGMP deviations, which may affect quality but no injuries have been reported.
Check the lot number on the container. If it matches HAVZC0020922, contact Aspen Biopharma for guidance.
The product was sold with an expiration date of August 2026.
We’ve drafted a message you can send Aspen Biopharma to request your refund or repair — edit it as you like.
Subject: Recall D-0265-2025 — Aspen Biopharma Aspen Biopharma Hello, I own a Aspen Biopharma that is covered by recall D-0265-2025 from Aspen Biopharma. 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.
