FDA Adverse Event Injury Summary report: N

ASR ACETABULAR CUPS 50

MDR report key: 3923873 · Received July 9, 2014

Report

Report Number
1818910-2014-23027
Event Type
Injury
Date Received
July 9, 2014
Date of Event
August 26, 2014
Report Date
August 26, 2014
Manufacturer
DEPUY INTL., 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
IL, US
Reporter Occupation
ATTORNEY

Narratives

Additional Manufacturer Narrative · 1

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

Additional Manufacturer Narrative · 1

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

Description of Event or Problem · 1

LITIGATION ALLEGES ELEVATED METAL ION LEVELS, PERMANENT INJURIES, AND PAIN.

Description of Event or Problem · 1

LITIGATION ALLEGES ELEVATED METAL ION LEVELS,PERMANENT INJURIES, AND PAIN.UPDATE 12 SEPT 2014 - ASR REVISION REPORTED VIA SALES REP. ADDED DOR. ((B)(6) 2014), PATIENT AGE, HEIGHT AND WEIGHT, SURGEON NAME, SALES REP DETAILS AND DETAILS FOR CUP, HEAD AND SLEEVE.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
402052 ASR ACETABULAR CUPS 50 HIP ACETABULAR CUP KWA DEPUY INTL., LTD. - 8010379 2275359

Patients

Seq Age Sex Outcome Treatment
1 68 YR Other| R