Aspen Biopharma recalls amber-colored Alprostadil bottles with lot HAALC002: CGMP deviations may affect safety. Check your product for recall.
CGMP Deviations
Aspen Biopharma is recalling amber-colored Alprostadil bottles due to manufacturing quality issues. This recall is important because the product may not meet safety standards.
CGMP deviations refer to manufacturing quality issues that could affect product safety. These deviations may mean the product does not meet the required safety standards.
People who own or use the amber-colored Alprostadil bottles with lot number HAALC0020922 are affected. Those using the product for medical purposes are at risk.
Check for amber-colored bottles with lot number HAALC0020922. The expiration date is August 2025.
Look for the amber color and lot number HAALC0020922 on the bottle.
The recall is due to CGMP deviations, which may affect safety, but the official notice does not specify the exact risk.
The recall record does not state a remedy, so no specific action is required beyond checking your product.
Check for the amber color and lot number HAALC0020922 on the bottle.
We’ve drafted a message you can send Aspen Biopharma to request your refund or repair — edit it as you like.
Subject: Recall D-0261-2025 — Aspen Biopharma Aspen Biopharma Hello, I own a Aspen Biopharma that is covered by recall D-0261-2025 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.
