FDA Adverse Event Injury Summary report: N

A AND H SPINBRUSH UNSPECIFIED

MDR report key: 15614986 · Received October 17, 2022

Report

Report Number
2280705-2022-01492
Event Type
Injury
Date Received
October 17, 2022
Report Date
September 28, 2022
Manufacturer
CHURCH & DWIGHT CO., INC
Product Code
JEQ
Adverse Event
Yes
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
MT, US
Reporter Occupation
OTHER

Narratives

Description of Event or Problem · 0

THIS SPONTANEOUS REPORT (2022-CDW-01492, 007628634A) FROM THE UNITED STATES OF AMERICA WAS REPORTED BY A MALE CONSUMER (GENDER UNSPECIFIED) WHOSE HEAD OF TOOTHBRUSH BROKE OFF AND HAD CHIPPED TOOTH COINCIDENT WITH A AND H SPINBRUSH UNSPECIFIED. THE CONSUMER'S MEDICAL HISTORY AND CONCOMITANT MEDICATIONS WERE NOT REPORTED. ON AN UNSPECIFIED DATE, THE CONSUMER INITIATED NEW A AND H SPINBRUSH UNSPECIFIED VIA DENTAL ROUTE. WHILE USING, THE OF IT BROKE OFF INTO HIS MOUTH AND CHIPPED HIS TOOTH. NO ADDITIONAL INFORMATION WAS AVAILABLE. THE ACTION TAKEN WITH A AND H SPINBRUSH UNSPECIFIED WAS UNKNOWN. THE OUTCOME OF THE EVENT CHIPPED MY TOOTH WAS UNKNOWN. THE OUTCOME OF THE EVENT HEAD OF IT BROKE OFF INTO MY MOUTH WAS NOT APPLICABLE.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
2944265 A AND H SPINBRUSH UNSPECIFIED TOOTHBRUSH, POWERED JEQ CHURCH & DWIGHT CO., INC

Patients

Seq Age Sex Outcome Treatment
1 Male Disability