FDA Adverse Event
Malfunction
Summary report: N
EMAX 2 PLUS MOTOR
MDR report key: 3811240
·
Received October 11, 2013
Report
- Report Number
- 1045834-2013-05092
- Event Type
- Malfunction
- Date Received
- October 11, 2013
- Date of Event
- September 17, 2012
- Report Date
- September 17, 2012
- Manufacturer
- DEPUY SYNTHES POWER TOOLS
- Product Code
- HBC
- PMA / PMN Number
- K080802
- Product Problem
- Yes
- Report Source
- Manufacturer report
- Reporter Location
- NJ, US
- Reporter Occupation
- OTHER
Narratives
Additional Manufacturer Narrative · 1
THE DEVICE WAS REC'D BY DEPUY SYNTHES POWER TOOLS. THE INVESTIGATION IS STILL IN PROCESS. ONCE THE INVESTIGATION HAS BEEN COMPLETED OR IF ADD'L INFO IS REC'D, A SUPPLEMENTAL REPORT WILL BE SENT. REF: (B)(4).
Description of Event or Problem · 1
REPORT REC'D FROM THE USA STATING THAT THE DEVICE WAS HEATING UP. THE DEVICE WAS BEING USED DURING EAR SURGERY, BUT THERE WAS NO INJURY OR MEDICAL INTERVENTION. IT IS UNK IF THERE WAS A DELAY IN SURGERY. THERE WAS NO ADD'L INFO PROVIDED.
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 524109 | EMAX 2 PLUS MOTOR | MOTOR, DRILL, ELECTRIC - HANDPIECE, PRODUCT CODE: HBC | HBC | DEPUY SYNTHES POWER TOOLS |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 |