Aspen Biopharma recalls amber bottle Latanoprost (NDC 82187-100: Lot HALAC0010123, exp Dec 2026; Lot HALAC0050923, exp Aug 2027) due to CGMP deviations. Consumers should check their bottles for lot numbers and expiration dates.
CGMP Deviations
Aspen Biopharma is recalling amber-colored Latanoprost eye drops with specific lot numbers and expiration dates because of manufacturing quality control issues. This recall is important because the product may not meet safety standards, potentially affecting the medication's effectiveness or safety.
CGMP deviations refer to failures in the manufacturing process that could lead to unsafe or ineffective medication. This means the eye drops might not work as intended or could cause adverse effects due to improper quality control.
People who own or use the recalled Latanoprost eye drops with the specified lot numbers and expiration dates are affected. Those with diabetes or other conditions requiring precise medication timing may be at higher risk.
Check the bottle for the amber color and the lot numbers HALAC0010123 (expires Dec 2026) or HALAC0050923 (expires Aug 2027). The product is sold under the brand name Latanoprost.
Look for lot numbers HALAC0010123 or HALAC0050923 on the bottle label.
The recall is due to CGMP deviations, which are manufacturing quality control issues that could affect the product's safety or effectiveness.
The official recall notice does not specify a remedy or action for consumers, so no specific steps are provided.
Check the bottle for the amber color and lot numbers HALAC0010123 (expires Dec 2026) or HALAC0050923 (expires Aug 2027).
We’ve drafted a message you can send Aspen Biopharma to request your refund or repair — edit it as you like.
Subject: Recall D-0264-2025 — Aspen Biopharma Aspen Biopharma Hello, I own a Aspen Biopharma that is covered by recall D-0264-2025 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.
