Alpha Aromatics recalls Pure Care Foaming Mint Hand Sanitizer 62% due to CGMP deviations. Consumers should check product lot numbers for affected batches.
CGMP Deviations
Alpha Aromatics is recalling Pure Care Foaming Mint Hand Sanitizer 62% because of CGMP deviations. This means the product may not meet safety standards and could pose risks.
CGMP deviations refer to failures in manufacturing quality control processes. This could mean the hand sanitizer does not meet safety standards and might not work as intended.
Anyone who owns or uses the Pure Care Foaming Mint Hand Sanitizer 62% with lot numbers 2022-012884, 2023-002020, 2023-003532, or 2023-003761. People using this product are most at risk.
Check the lot number on the product label. Affected lots are 2022-012884, 2023-002020, 2023-003532, and 2023-003761. The product is distributed by Air Scent International.
Look for the lot number on the product label to determine if it is affected.
The recall is due to CGMP deviations, which means the product may not meet safety standards. It is not recommended for use until the recall is resolved.
Check the lot number on the label. Affected lots are 2022-012884, 2023-002020, 2023-003532, and 2023-003761.
The recall does not specify a remedy, so check the official recall notice for further instructions.
We’ve drafted a message you can send Alpha Aromatics to request your refund or repair — edit it as you like.
Subject: Recall D-0338-2024 — Alpha Aromatics Alpha Aromatics Hello, I own a Alpha Aromatics that is covered by recall D-0338-2024 from Alpha Aromatics. 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.
