FDA Adverse Event
Malfunction
Summary report: N
CORE IMPACTION DRILL
MDR report key: 3182025
·
Received June 21, 2013
Report
- Report Number
- 0001811755-2013-01450
- Event Type
- Malfunction
- Date Received
- June 21, 2013
- Date of Event
- May 30, 2013
- Report Date
- May 30, 2013
- Manufacturer
- STRYKER INSTRUMENTS-KALAMAZOO
- Product Code
- DZJ
- PMA / PMN Number
- K040369
- Product Problem
- Yes
- Report Source
- Manufacturer report
- Reporter Location
- AL, US
- Reporter Occupation
- OTHER
Narratives
Additional Manufacturer Narrative · 1
DEVICE EVALUATION WILL BEGIN WHEN THE DEVICE IS RECEIVED. DEVICE EVALUATION WILL BEGIN WHEN THE DEVICE IS RECEIVED.
Additional Manufacturer Narrative · 1
THE REPORTED EVENT WAS DUPLICATED. UPON DISASSEMBLY FOR VISUAL INSPECTION THE SERVICE TECHNICIAN OBSERVED A COUPLER WORN.
Description of Event or Problem · 1
IT WAS REPORTED THAT THE CORE IMPACTION DRILL HEATED UP. NO FURTHER INFORMATION WAS PROVIDED.
Description of Event or Problem · 1
IT WAS REPORTED THAT THE CORE IMPACTION DRILL HEATED UP. NO FURTHER INFORMATION WAS PROVIDED.
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 282191 | CORE IMPACTION DRILL | DRIVER, WIRE, AND BONE DRILL, MANUAL | DZJ | STRYKER INSTRUMENTS-KALAMAZOO |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 |