Aspen Biopharma recalls bimatoprost (NDC 82187-1001-1) due to CGMP deviations. Affected lots expire Dec-2026 to Sep-2028. Consumers should check lot numbers on packaging.
CGMP Deviations
Aspen Biopharma is recalling bimatoprost eye drops with specific lot numbers due to manufacturing quality control issues. This recall means the product may not meet safety standards, so affected users should stop using it and contact the company.
CGMP deviations refer to failures in the manufacturing process that could affect product safety and quality. This means the bimatoprost may not be as effective or safe as it should be, potentially leading to health issues if used improperly.
People who purchased bimatoprost eye drops with lot numbers HABTC0020123 (expires Dec-2026), HABTC0050623 (expires May-2027), or HABTC0091023 (expires Sep-2028) are affected. Those using the product for glaucoma or eye pressure management are most at risk.
Check the lot number on the packaging, which is listed as HABTC0020123, HABTC0050623, or HABTC0091023. The product expires by Dec-2026, May-2027, or Sep-2028 respectively.
Look for the lot number on the packaging: HABTC0020123, HABTC0050623, or HABTC0091023.
If the lot number matches, stop using the bimatoprost immediately.
Aspen Biopharma is recalling bimatoprost eye drops with specific lot numbers due to manufacturing quality control issues.
Check the lot number on the packaging: HABTC0020123 (expires Dec-2026), HABTC0050623 (expires May-2027), or HABTC0091023 (expires Sep-2028).
If you have the recalled product, stop using it immediately and contact Aspen Biopharma for further instructions.
We’ve drafted a message you can send Aspen Biopharma to request your refund or repair — edit it as you like.
Subject: Recall D-0260-2025 — Aspen Biopharma Aspen Biopharma Hello, I own a Aspen Biopharma that is covered by recall D-0260-2025 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.
