CHURCH & DWIGHT CO., INC.
180 adverse events · 24 recalls · 23 clearances · 17 inspections · 2 compliance actions · aggregated across 3 source records
Scorecard
Events per device across the 260-device portfolio, trailing 12 months. Arrows compare the last 90 days with the 90 before.
MAUDE reports per device
0.077 →
20 in the last 12 months
Higher volume than 93% of companies with 10+ devices
Recalls per device
0 →
0 in the last 12 months
Higher volume than 97% of companies with 10+ devices
These are reporting-volume percentiles, not safety rankings — MAUDE counts have no denominator of devices in use, and recall attribution follows resolved links. A high percentile means more reports per registered device than peers, which can reflect market size, device criticality, or reporting practice as much as anything else.
Devices
260 device records · ordered by linked event volume.
Showing 1–30 of 260Next →
Compliance actions
FDA warning letters and enforcement actions (full history).
| Date | Type | Action | Firm |
|---|---|---|---|
| 2011-05-16 | WL | Warning Letter | Church & Dwight Inc |
| 2011-05-16 | WL | Warning Letter | Church & Dwight Inc |
Facilities
Registered establishments with their latest FDA inspection outcome.
| FEI | Name | Location | Last inspection | Watch |
|---|---|---|---|---|
| 2280705 | CHURCH & DWIGHT CO., INC. | PRINCETON, NJ, US | NAI | |
| 1000657351 | Church & Dwight Canada Corp. | MONTREAL, QUEBEC, CA | NAI | |
| 1122329 | Church & Dwight Manufacturing Co., Inc. | South Chesterfield, VA, US | NAI |