FDA Adverse Event Injury Summary report: N

DEPUY ASR XL FEM IMP SIZE 45

MDR report key: 3102573 · Received May 9, 2013

Report

Report Number
1818910-2013-05601
Event Type
Injury
Date Received
May 9, 2013
Date of Event
October 21, 2011
Report Date
November 2, 2015
Manufacturer
DEPUY INTERNATIONAL LTD - 8010379
Product Code
KWA
Removal / Correction Number
Z-1749/1816-2011
Adverse Event
Yes
Report Source
Manufacturer report
Reporter Location
UK
Reporter Occupation
ATTORNEY

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

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

ASR REVISION; ASR XL - RIGHT HIP; REASON FOR REVISION: UNKNOWN.

Description of Event or Problem · 1

UPDATE 5 NOV. 2015: UPDATED REASON FOR REVISION AS PAIN AND ALVAL / SOFT TISSUE REACTION, ADDED MANUFACTURE AND EXPIRY DATES FOR PRODUCTS, UPDATED FILE HANDLER DETAILS. TAKEN FROM SCF 3 NOV. 2015.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
203141 DEPUY ASR XL FEM IMP SIZE 45 HIP FEMORAL HEAD KWA DEPUY INTERNATIONAL LTD - 8010379 2441585

Patients

Seq Age Sex Outcome Treatment
1 Required Intervention