Little Moon Essentials recalls Ass Kisser products with CGMP deviations. Affected items include 0.5 oz and 3 oz metal tins with specific UPCs and lot codes. No remedy provided in recall notice.
CGMP deviations
Little Moon Essentials is recalling their Ass Kisser products due to CGMP deviations. This means the products may not meet quality and safety standards, though the exact risk isn't specified in the recall notice.
CGMP deviations refer to failures in manufacturing quality control processes. This could mean the product doesn't meet safety standards, but the recall doesn't specify the exact hazard or how it might affect users.
Owners of the Ass Kisser products with specific UPC codes and lot numbers listed in the recall notice. People using these products for personal lubrication or similar purposes.
Check for the 0.5 oz (14g) metal tin with UPC 673673882282 or the 3 oz (85.05g) metal tin with UPC 673673882084. Lot codes 327140 or 322170, 325040, 325250 are also affected.
Identify the UPC code and lot number on the product to confirm if it's affected.
The recall is due to CGMP deviations, which are failures in manufacturing quality control processes. The exact risk isn't specified in the notice.
The recall notice does not provide a remedy, so there's no action required beyond checking if your product is affected.
Yes, lot codes 327140, 322170, 325040, and 325250 are affected.
We’ve drafted a message you can send Little Moon Essentials to request your refund or repair — edit it as you like.
Subject: Recall D-0576-2024 — Little Moon Essentials Little Moon Essentials Hello, I own a Little Moon Essentials that is covered by recall D-0576-2024 from Little Moon Essentials. 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.