FDA Adverse Event Injury Summary report: N

DEPUY ASR XL FEM IMP SIZE 53

MDR report key: 3061050 · Received April 16, 2013

Report

Report Number
1818910-2013-04912
Event Type
Injury
Date Received
April 16, 2013
Date of Event
March 12, 2013
Report Date
March 7, 2014
Manufacturer
DEPUY INTERNATIONAL
Product Code
KWA
Removal / Correction Number
Z- 1749/1816-2011
Adverse Event
Yes
Report Source
Manufacturer report
Reporter Location
US
Reporter Occupation
PATIENT

Narratives

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. REF. (B)(4). DEPUY CONSIDERS THE INVESTIGATION CLOSED AT THIS TIME. SHOULD THE PRODUCT AND/OR ADDITIONAL INFORMATION BE RECEIVED, THE INVESTIGATION WILL BE RE-OPENED. THE CORRECTION/REMOVAL REPORTING NUMBER LISTED APPLIES TO THE CORRESPONDING PRODUCT CODE SOLD DOMESTICALLY.

Additional Manufacturer Narrative · 1

DEPUY STILL CONSIDERS THE INVESTIGATION CLOSED. ADDITIONAL NARRATIVE: IF INFORMATION IS OBTAINED THAT WAS NOT AVAILABLE FOR THE INITIAL MEDWATCH, A FOLLOW-UP MEDWATCH WILL BE FILED AS APPROPRIATE.

Description of Event or Problem · 1

ASR REVISION, ASR XL ACETABULAR SYSTEM - RIGHT; REASON(S) FOR REVISION: ALVAL / SOFT TISSUE REACTION.

Description of Event or Problem · 1

NEW ETQ RECORD CREATED IN ORDER TO UPDATE ETQ (LEGACY SYSTEM) COMPLAINT (B)(4). REASON FOR ORIGINAL COMPLAINT ¿ ASR REVISION; ASR XL ACETABULAR SYSTEM - RIGHT; REASON(S) FOR REVISION: ALVAL / SOFT TISSUE REACTION. UPDATE RECEIVED (B)(4) 2014. ADDITIONAL SURGEON ADDED. STEM, KID ADDED. STATUS CHANGED TO LEGAL.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
162880 DEPUY ASR XL FEM IMP SIZE 53 HIP FEMORAL HEAD KWA DEPUY INTERNATIONAL 2120364

Patients

Seq Age Sex Outcome Treatment
1 Required Intervention