RegWardenFDA facility compliance records
Company

CHURCH & DWIGHT CO., INC.

3 recall(s) on record — most severe on record: Class II.

Recalls by year

FDA actions on record by year2011: 1 recalls; 2013: 1 recalls; 2023: 1 recalls1’11’121’13’14’15’16’17’18’19’20’21’221’23’24’25’26
  • Recalls (3)

Registered facilities (3)

Recalls & enforcement

  • Class IIOngoing2023-01-25
    Church & Dwight First Response Pregnancy Kits was marketed with the Easy Read App without a new 510k. There is also a potential for Easy Read App to be unable to reads the test results (i.e., no results reported on the APP screen) or to misread the analog results shown on the pr…
  • Class IITerminated2013-06-11
    Church and Dwight Co., Inc. has initiated a recall for Sodium Bicarbonate, USP produced by the Old Fort, OH Sodium Bicarbonate Production facility due to metal and other contamination.
  • Class IITerminated2011-12-22
    Church and Dwight plans to take actions to best convey to the public the potential small parts choking hazard with using a Spinbrush beyond the recommended 3-month brush head life.

Source: U.S. FDA via openFDA (opens in a new tab) (device registration & enforcement). Data as of 2026-10-06. We restate the public record only — measured facts, never risk verdicts.

Cite this record

RegWarden. “CHURCH & DWIGHT CO., INC. — FDA compliance profile.” Compiled from U.S. FDA public records (openFDA; FDA Data Dashboard). Data as of 2026-10-06. https://regwarden.com/company/oo-2210299-church-dwight-co-inc/

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