Church & Dwight — FDA Recall History & Enforcement Records
Data Notice: Recall frequency varies by category and firm size; data is comparative and may not indicate actual brand safety or quality. See Methodology.
As of July 22, 2026, Church & Dwight has 3 recorded FDA food enforcement actions in the openFDA database. Their most recent recall was on 17 Aug 2018. Church & Dwight is categorized under Supplements & Specialty based on their predominant recall history.
Recall activity over time for Church & Dwight
How serious are Church & Dwight recalls?
FDA recall classifications by severity
Full FDA recall history for Church & Dwight
All 3 FDA enforcement actions sourced from openFDA · Sorted by date, most recent first
| Date | Product | Reason | Class & Status |
|---|---|---|---|
| 17 Aug 2018Official FDA Notice | Trader Darwin s Chewable Peppermint Flavored Melatonin Dietary Supplement Number of units per package: 100 tablets Pack | Product is misbranded. Bottles contain another product -GABA Calm Sublingual Orange tablets. | Class IITerminated |
| 4 Jun 2015Official FDA Notice | Gummy Vites Complete Multivitamin L’il Critters 70 gummies Manufactured for Church & Dwight Co., Inc. Ewing, NJ 08628 | Two lots of Lil Critters GummyVite 70 ct were produced using the Adult Multivitamin bulk. | Class IITerminated |
| 12 Jun 2013Official FDA Notice | Arm & Hammer Baking Soda a) Net Wt. 1 LB. (454 g) UPC 3320001130 b) Net Wt. 8 oz. (277 g) UPC 3320001110 Church & Dw | Church and Dwight Co., Inc. has initiated a recall for Sodium Bicarbonate, USP produced by the Old Fort, OH Sodium Bicarbonate Production facility due | Class IITerminated |
Where have Church & Dwight recalls occurred?
States affected across all recorded FDA enforcement actions
Where does this recall data come from?
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Data sourced from the FDA Recall Enterprise System via openFDA API. This information is for educational purposes only and does not constitute health or legal advice. FoodRecallFinder.com is not affiliated with or endorsed by the U.S. Food and Drug Administration.
To determine if your specific product is affected, verify that the brand name, product description, lot number, UPC code, and date range all match the recall details exactly. When in doubt contact the recalling firm or visit FDA.gov.
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