Alpha Aromatics recalls 1-gallon mint-scented hand sanitizer with 62% alcohol due to FDA-detected acetaldehyde and acetal levels exceeding safety limits. No expiration date on labels.
CGMP Deviations: FDA analysis found product to contain acetaldehyde and acetal above specification limits.
Alpha Aromatics is recalling mint-scented hand sanitizer bottles that contain acetaldehyde and acetal above safe levels. This could pose a risk to health if used as intended.
The hand sanitizer contains acetaldehyde and acetal levels higher than FDA specifications. These chemicals can cause irritation or allergic reactions in some users, but the risk is not severe enough to cause serious injury.
People who own or use the recalled hand sanitizer bottles with the specific lot numbers listed. Those with sensitive skin or respiratory issues may be at slightly higher risk.
Check for the mint-scented hand sanitizer with 62% alcohol, 1-gallon size, and lot numbers 2020-013211 or 2020-013629. The product has no expiration date on the label.
Identify the lot numbers 2020-013211 or 2020-013629 on the label to confirm if your product is recalled.
The FDA found higher levels of acetaldehyde and acetal than allowed, which could cause irritation or allergic reactions in some people, but it is not considered a serious health risk.
Check the lot numbers on the label. If it matches 2020-013211 or 2020-013629, contact Alpha Aromatics for instructions.
The recall notice does not specify a deadline for action.
We’ve drafted a message you can send Alpha Aromatics to request your refund or repair — edit it as you like.
Subject: Recall D-0760-2023 — Alpha Aromatics Alpha Aromatics Hello, I own a Alpha Aromatics that is covered by recall D-0760-2023 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.
Experiences, tips, and questions from readers. Every comment is reviewed before it appears.
No comments yet — be the first to share your experience.
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.