Lower riskFood recall · FDA · Published June 4, 2015
Church & Dwight Gummy Vites L'il Critters Multivitamin Recall: Adult Multivitamin Used
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.
“Church & Dwight Gummy Vites L'il Critters Multivitamin Recall: Adult Multivitamin Used.” GovInfoNow, updated August 18, 2026. https://govinfonow.com/recall/26790-church-dwight-gummy-vites-l-il-critters-multivitamin-recall-adult. Based on FDA recall #F-2931-2015 (https://api.fda.gov/food/enforcement.json?search=recall_number:%22F-2931-2015%22&limit=1).
Church & Dwight Inc recalled L'il Critters GummyVites Complete Multivitamin 70 gummies due to potential adult multivitamin bulk contamination, according to the FDA on June 4, 2015.
Two lots of the product were produced using Adult Multivitamin bulk. The FDA classified this as a Class II recall.
Context
GovInfoNow's records show Church & Dwight Inc has had five other recalls on record since September 6, 2012. Other recent recalls of similar products include ZICAM Cold Remedy Nasal Swabs Recall (June 6, 2025), TheraBreath for Kids Recall (September 8, 2023), and First Response Pregnancy Test Sticks recall (January 25, 2023).
How to tell if you have this one
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.
Brand
Church & Dwight
Category
Food
Based on the official FDA remedy
What to do — step by step
Check Product Lot Code
Look for the lot code WA50459364 on the packaging to identify if the product is recalled.
Where it went and when
Where it was distributed
Distributed in New Jersey.
Listed by the agency
Not listed
FDA distribution: “NJ” States read from FDA’s own wording; “not listed” means the notice does not name it.
States: New Jersey.
Recall timeline
FDA terminated this recall 2 years after the firm started it.
1Firm started the recall
2FDA classified it Class II
3Published in FDA’s Enforcement Report
4FDA terminated the recall
Dates from the agency record only; steps without a date are left out.
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.
Official source: FDA Recall #F-2931-2015 (June 4, 2015) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for F-2931-2015 to see it in context.
Plain-language summary written by qwen3:4b on August 18, 2026, from the official record above. Not reviewed by a person — if it conflicts with the FDA notice, the notice is correct. Report an error on this page.
GovInfoNow is an independent service and is not a government agency. We republish official FDA recall data; we don’t issue, amend or administer recalls.