FDA Adverse Event Injury Summary report: N

CORAIL2 NON COL HO SIZE 14

MDR report key: 2210362 · Received August 8, 2011

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

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.

Additional Manufacturer Narrative · 1

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 Manufacturer Narrative · 1

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.

Description of Event or Problem · 1

THE PATIENT WAS REVISED TO ADDRESS PAIN.

Description of Event or Problem · 1

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