CORAIL2 NON COL HO SIZE 14
Report
- Report Number
- 1818910-2011-15102
- Event Type
- Injury
- Date Received
- August 8, 2011
- Date of Event
- July 11, 2011
- Report Date
- August 1, 2014
- Manufacturer
- DEPUY FRANCE SAS-3003895575
- Product Code
- KWA
- PMA / PMN Number
- K042992
- Removal / Correction Number
- Z-1749/1816-2011
- Adverse Event
- Yes
- Report Source
- Manufacturer report
- Reporter Location
- SF
- Reporter Occupation
- PATIENT
Narratives
THIS COMPLAINT IS STILL UNDER INVESTIGATION. DEPUY WILL NOTIFY THE FDA OF THE RESULTS OF THIS INVESTIGATION ONCE IT HAS BEEN COMPLETED.
THE ASR PLATFORM WAS VOLUNTARILY RECALLED FROM THE MARKET IN AUGUST 2010, AND THE ASR PRODUCT CODES ARE NOW CONSIDERED INACTIVE. FURTHER INVESTIGATION OF THIS INDIVIDUAL INCIDENT WILL NOT BE UNDERTAKEN, AS THERE IS AN ONGOING INVESTIGATION REGARDING THE ROOT CAUSE(S) AND/OR CORRECTIVE ACTIONS. (B)(4).
ADDITIONAL NARRATIVE: IF INFORMATION IS OBTAINED THAT WAS NOT AVAILABLE FOR THE INITIAL MEDWATCH, A FOLLOW-UP MEDWATCH WILL BE FILED AS APPROPRIATE. DEPUY STILL CONSIDERS THIS CASE CLOSED TO CAPA.
THE PATIENT WAS REVISED TO ADDRESS PAIN.
NEW ETQ RECORD CREATED IN ORDER TO UPDATE ETQ (LEGACY SYSTEM) COMPLAINT NUMBER (B)(4). REASON FOR ORIGINAL COMPLAINT ¿ ASR REVISION; ASR HIP RESURFACING SYSTEM (LEFT); REASON FOR REVISION: PAIN. UPDATE RECEIVED 1ST AUGUST 2014. HOSPITAL AND SURGEON NAMES AMENDED. STATUS AMENDED TO "LEGAL". KID NUMBER ADDED.
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 1 | CORAIL2 NON COL HO SIZE 14 | HIP FEMORAL STEM/SLEEVE | KWA | DEPUY FRANCE SAS-3003895575 | NA | 2467366 |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 | NA | Required Intervention |