FDA Adverse Event
Injury
Summary report: N
ELECTROTORQUE PLUS
MDR report key: 617464
·
Received June 24, 2005
Report
- Report Number
- 1419798-2005-00002
- Event Type
- Injury
- Date Received
- June 24, 2005
- Date of Event
- January 1, 2005
- Report Date
- January 14, 2005
- Manufacturer
- KAVO DENTAL
- Product Code
- EKK
- Adverse Event
- Yes
- Report Source
- Manufacturer report
- Reporter Location
- IL, US
- Reporter Occupation
- DENTIST
Narratives
Description of Event or Problem · 1
A DENTIST REPORTED THAT A PT RECEIVED A BURN ON THE INSIDE OF THEIR CHEEK DURING THE USE OF A 25LHA HANDPIECE. IT WAS REPORTED THAT THE BURN RESULTED IN A BLISTER. THE PT WAS ADMINISTERED ANTIBIOTICS (ROUTE AND DOSE UNKNOWN) AND AN UNKNOWN OINTMENT WAS APPLIED TO THE BURN. IT WAS REPORTED THAT THE PT WAS RECOVERED.
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 1 | ELECTROTORQUE PLUS | ELECTRIC DENTAL HANDPIECE | EKK | KAVO DENTAL | 25LHA | NA |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 | UNKNOWN | Other |