FDA Adverse Event Injury Summary report: N

TOTAL ASR ACET IMP SIZE 54

MDR report key: 3363756 · Received September 24, 2013

Report

Report Number
1818910-2013-28297
Event Type
Injury
Date Received
September 24, 2013
Date of Event
July 15, 2011
Report Date
November 4, 2013
Manufacturer
DEPUY INTL., LTD. - 8010379
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 THIS COMPLAINT CLOSED TO CAPA.

Additional Manufacturer Narrative · 1

NO 510(K) NUMBER PROVIDED BECAUSE THIS IMPLANT IS SOLD INTERNATIONALLY WITH DIFFERENT INDICATIONS FOR USE; IT IS CURRENTLY SOLD IN THE U.S. UNDER A DIFFERENT PART NUMBER. THE CORRECTION/REMOVAL REPORTING NUMBER LISTED APPLIES TO THE CORRESPONDING PRODUCT CODE SOLD DOMESTICALLY. 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.

Additional Manufacturer Narrative · 1

DEPUY STILL CONSIDERS THE INVESTIGATION CLOSED.

Additional Manufacturer Narrative · 1

DEPUY STILL CONSIDERS THE INVESTIGATION CLOSED. SHOULD ADDITIONAL INFORMATION BE RECEIVED THE INVESTIGATION WILL BE REOPENED.

Description of Event or Problem · 1

ASR REVISION; ASR XL- RIGHT; REASON(S) FOR REVISION: NOISE; ALVAL/SOFT TISSUE DAMAGE. *****BI-LATERAL - SEE COM 023126 FOR LEFT HIP.*****

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
480807 TOTAL ASR ACET IMP SIZE 54 ACETABULAR CUP KWA DEPUY INTL., LTD. - 8010379 2293540

Patients

Seq Age Sex Outcome Treatment
1 Required Intervention