Church & Dwight recalls L'il Critters 70-count gummies made with adult multivitamin ingredients. This could cause incorrect dosing for children. Consumers should check lot codes and contact the company for details.
Two lots of Lil Critters GummyVite 70 ct were produced using the Adult Multivitamin bulk.
Church & Dwight is recalling L'il Critters 70-count gummy multivitamins because they were made using adult multivitamin ingredients. This could lead to incorrect dosing for children who eat them.
The gummies were produced using adult multivitamin ingredients instead of child-safe ones. This means children might get too many vitamins or other ingredients they shouldn't have.
Children who eat the gummies are at risk of incorrect dosing. Parents or caregivers of young children who bought these gummies should check if they have the recalled product.
Check the lot code on the packaging. The recalled product has lot code WA50459364 and was manufactured in Ewing, NJ. The product is sold as L'il Critters 70 gummies.
Look for the lot code WA50459364 on the packaging to identify if the product is recalled.
The gummies were made using adult multivitamin ingredients instead of child-safe ones, which could lead to incorrect dosing for children.
Check the lot code on the packaging; the recalled product has lot code WA50459364 and was manufactured in Ewing, NJ.
The recall record does not specify a remedy, so contact Church & Dwight directly for instructions.
We’ve drafted a message you can send Church & Dwight to request your refund or repair — edit it as you like.
Subject: Recall F-2931-2015 — Church & Dwight Church & Dwight Hello, I own a Church & Dwight that is covered by recall F-2931-2015 from Church & Dwight. 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.
