FDA Adverse Event Injury Summary report: N

ASR ACETABULAR CUPS 50

MDR report key: 4091001 · Received September 16, 2014

Report

Report Number
1818910-2014-28101
Event Type
Injury
Date Received
September 16, 2014
Date of Event
August 29, 2014
Report Date
December 10, 2014
Manufacturer
DEPUY INTERNATIONAL LTD.-8010379
Product Code
KWA
PMA / PMN Number
PK040627
Removal / Correction Number
Z-1749/1816-2011
Adverse Event
Yes
Report Source
Manufacturer report
Reporter Location
CO, US
Reporter Occupation
PHYSICIAN

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. (B)(4). DEPUY CONSIDERS THIS INVESTIGATION CLOSED AT THIS TIME. SHOULD THE PRODUCT AND/OR ADDITIONAL INFORMATION BE RECEIVED, THE INVESTIGATION WILL BE RE-OPENED.

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.(B)(4). DEPUY STILL CONSIDERS THIS INVESTIGATION CLOSED.

Description of Event or Problem · 1

ASR REVISION REPORTED VIA SALES REP; LEFT; REASON(S) FOR REVISION : PAIN / ELEVATED ION LEVELS.

Description of Event or Problem · 1

UPDATE REC'D 12/10/2014- LITIGATION PAPERS RECEIVED. LITIGATION ALLEGES PAIN, DISCOMFORT, FLUID ABNORMALITIES, DECREASED RANGE OF MOTION. MUSCLE MASS DETERIORATION OF SOFT TISSUE, AND ELEVATED METAL ION LEVELS. THE DOB WAS PROVIDED. THE STEM IS BEING ADDED BECAUSE OF ELEVATED METAL ION LEVELS. THE COMPLAINT WAS UPDATED ON: 01/27/2014.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
570978 ASR ACETABULAR CUPS 50 HIP ACETABULAR CUP KWA DEPUY INTERNATIONAL LTD.-8010379 2467411

Patients

Seq Age Sex Outcome Treatment
1 73 YR Required Intervention