FDA Adverse Event
Injury
Summary report: N
CORAIL2 LAT COXA VARA SIZE 9
MDR report key: 1040122
·
Received May 7, 2008
Report
- Report Number
- 1818910-2008-01566
- Event Type
- Injury
- Date Received
- May 7, 2008
- Date of Event
- April 9, 2008
- Report Date
- April 8, 2008
- Manufacturer
- DEPUY FRANCE S.A.
- Product Code
- KWA
- PMA / PMN Number
- K042992
- Removal / Correction Number
- NA
- Adverse Event
- Yes
- Report Source
- Manufacturer report
- Reporter Location
- FR
- Reporter Occupation
- OTHER
Narratives
Additional Manufacturer Narrative · 1
THIS COMPLAINT IS STILL UNDER INVESTIGATION. DEPUY WILL NOTIFY THE FDA OF THE RESULTS OF THIS INVESTIGATION ONCE IT HAS BEEN COMPLETED.
Description of Event or Problem · 1
NECK FRACTURE OF CORAIL STEM KLA9.
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 1 | CORAIL2 LAT COXA VARA SIZE 9 | 87KWA | KWA | DEPUY FRANCE S.A. | NA | 367227 |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 | NA | Required Intervention |