FDA Adverse Event Injury Summary report: N

TOTAL ASR ACET IMP SIZE 54

MDR report key: 2780349 · Received October 10, 2012

Report

Report Number
1818910-2012-76141
Event Type
Injury
Date Received
October 10, 2012
Date of Event
June 26, 2012
Report Date
March 26, 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

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

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). 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.

Description of Event or Problem · 1

ASR REVISION; LEFT ASR HIP RESURFACING; REASON FOR REVISION: ALVAL/SOFT TISSUE REACTION; PAIN.

Description of Event or Problem · 1

NEW ETQ RECORD CREATED IN ORDER TO UPDATE ETQ (LEGACY SYSTEM) (B)(4). REASON FOR ORIGINAL COMPLAINT: ASR REVISION, LEFT, ASR HIP RESURFACING, REASON(S) FOR REVISION: ALVAL / SOFT TISSUE REACTION & PAIN. UPDATE RECEIVED: 26TH MARCH 2014 - ADDED FURTHER REASON(S) FOR REVISION: ENORMOUSLY RAISED METAL IONS AND LYSIS AND ATTACHED SURGEON CONFIRMATION FORM.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1 TOTAL ASR ACET IMP SIZE 54 HIP ACETABULAR CUP KWA DEPUY INTERNATIONAL 2568297

Patients

Seq Age Sex Outcome Treatment
1 Required Intervention