FDA Adverse Event
Injury
Summary report: N
A AND H SPINBRUSH UNSPECIFIED
MDR report key: 19381680
·
Received May 23, 2024
Report
- Report Number
- 2280705-2024-00825
- Event Type
- Injury
- Date Received
- May 23, 2024
- Report Date
- May 23, 2024
- Manufacturer
- CHURCH & DWIGHT CO., INC
- Product Code
- JEQ
- Adverse Event
- Yes
- Report Source
- Manufacturer report
- Reporter Occupation
- OTHER
Narratives
Description of Event or Problem · 0
THIS SPONTANEOUS REPORT (2024-CDW-00825, 06922190) FROM THE UNITED STATES OF AMERICA WAS REPORTED BY A CONSUMER (AGE AND GENDER UNSPECIFIED) WHO HAD CHIPPED TEETH WHILE USING THE A AND H SPINBRUSH UNSPECIFIED. ON AN UNSPECIFIED DATE, THE CONSUMER INITIATED THE A AND H SPINBRUSH UNSPECIFIED VIA THE DENTAL ROUTE. WHILE USING IT, THE CONSUMER'S FRONT TEETH GOT CHIPPED. NO ADDITIONAL INFORMATION WAS AVAILABLE. THE ACTION TAKEN WITH A AND H SPINBRUSH UNSPECIFIED, AND THE OUTCOME OF THE EVENT WAS UNKNOWN.
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 516183 | A AND H SPINBRUSH UNSPECIFIED | A AND H SPINBRUSH UNSPECIFIED | JEQ | CHURCH & DWIGHT CO., INC |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 | NA | Unknown | Required Intervention |