Lil Critters Gummy Vites Recalled for Incorrect Bulk Ingredient Use
Church & Dwight is recalling Lil Critters Gummy Vites Complete Multivitamin because two lots were produced using Adult Multivitamin bulk.
What this means for you
Minor labeling or packaging issue, or a voluntary precautionary recall. Risk of harm is low but real — follow the manufacturer's instructions.
Our severity reasoning: The recall is classified as FDA Class II, which typically involves a low probability of serious adverse health consequences. The hazard is a manufacturing error involving the use of incorrect bulk material, which falls under moderate severity criteria for labeling or formulation errors without reported illness.
Plain-English summary
Church & Dwight Inc. is recalling Lil Critters Gummy Vites Complete Multivitamin, 70 gummies. The recall involves 3,360 bottles distributed in New Jersey. The specific lot code is WA50459364.
The recall was initiated because two lots of the product were produced using Adult Multivitamin bulk instead of the intended ingredient. This constitutes a manufacturing error regarding the bulk material used in the production process.
Consumers who have purchased this product should check their lot codes. If the lot code matches WA50459364, they should stop using the product and contact the manufacturer for instructions on disposal or return.
The recalled product
- Product
- Gummy Vites Complete Multivitamin L'il Critters 70 gummies Manufactured for Church & Dwight Co., Inc. Ewing, NJ 08628
- Manufacturer
- Church & Dwight Inc
- Category
- Food — Dietary Supplement
- Affected units
- 3,360
Is your product affected?
Check your packaging against the codes below. If any of them match, the product is part of this recall.
Lot numbers (1)
- Lot Code WA50459364
Distribution
Distributed in 1 state:
Related recalls
Same manufacturer · Church & Dwight Inc
See all →- SevereZicam cold remedy nasal swabs recalled over fungal contamination
FDA (Drugs) · 2025-07-09
- SevereZicam Nasal AllClear swabs recalled over fungal contamination of swabs
FDA (Drugs) · 2025-07-09
- SevereOrajel Baby teething swabs recalled over fungal contamination of swabs
FDA (Drugs) · 2025-07-09
- SevereTheraBreath for Kids Oral Rinse Recalled for Yeast Contamination
FDA (Drugs) · 2023-10-25
- HighFirst Response Easy Read App unable to reliably read pregnancy test results
FDA (Devices) · 2023-04-19
Same hazard · mis labeling
See all →- ModerateOlympus Recalls PowerSeal Sealer Due to Incorrect Outer Box Labeling
FDA (Devices) · 2026-09-02
- ModerateAVID Medical Recalls Halyard Total Joint Kits for Latex Labeling Deficiency
FDA (Devices) · 2026-09-02
- HighByron White A-L Complex Herbal Supplement Recalled for Undeclared Walnut
FDA (Food) · 2026-09-02
- ModerateMedline Trach Tube Kit Recalled for Component Labeling Discrepancy
FDA (Devices) · 2026-09-02
- SevereWhite Vein Advanced Alkaloids Chewable Tablets Recall for Excess Active Ingredient
FDA (Food) · 2026-09-02