FDA Adverse Event
Malfunction
Summary report: N
CORE IMPACTION DRILL
MDR report key: 2043353
·
Received March 15, 2011
Report
- Report Number
- 1811755-2011-00817
- Event Type
- Malfunction
- Date Received
- March 15, 2011
- Date of Event
- February 16, 2011
- Report Date
- February 16, 2011
- Manufacturer
- STRYKER INSTRUMENTS KALAMAZOO
- Product Code
- DZJ
- PMA / PMN Number
- K040369
- Product Problem
- Yes
- Report Source
- Manufacturer report
- Reporter Location
- MS, US
- Reporter Occupation
- UNKNOWN
Narratives
Additional Manufacturer Narrative · 1
DURING THE QUALITY INVESTIGATION, THE CUSTOMER'S COMPLAINT WAS CONFIRMED; THE DEVICE OVERHEATED DURING TESTING. FURTHER INVESTIGATION REVEALED A BROKEN ROTOR AND OTHER COMPONENT PARTS. THE MOTOR CARTRIDGE HAD NO POWER. CORROSION DAMAGE WAS IDENTIFIED AS THE ROOT CAUSE OF THE DEVICE FAILURE. THE PARTS WERE REPLACED AND THE DEVICE WAS REPAIRED AND RETURNED TO THE CUSTOMER.
Description of Event or Problem · 1
A STRYKER CORE IMPACTION DRILL WAS CALLED IN FOR REPAIR DUE TO OVERHEATING DURING A TOOTH EXTRACTION. THE PROCEDURE WAS COMPLETED WITH ANOTHER DEVICE, NO ADVERSE EVENT WAS REPORTED.
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 1 | CORE IMPACTION DRILL | BONE CUTTING INSTRUMENT AND ACCESSORIES | DZJ | STRYKER INSTRUMENTS KALAMAZOO |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 | UNK |