FDA Adverse Event Injury Summary report: N

ASR UNI FEMORAL IMPL SIZE 45

MDR report key: 3183235 · Received June 21, 2013

Report

Report Number
1818910-2013-19568
Event Type
Injury
Date Received
June 21, 2013
Date of Event
April 2, 2015
Report Date
April 2, 2015
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
TX, US
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.

Additional Manufacturer Narrative · 1

THERE IS NO NEW INFORMATION THAT WOULD CHANGE THE OUTCOME OF THE INVESTIGATION. THE COMPLAINT IS CONSIDERED CLOSED.

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 THE INVESTIGATION CLOSED.

Description of Event or Problem · 1

LITIGATION PAPERS RECEIVED ALLEGING THAT THE PATIENT SUFFERS FROM PAIN, ACHING IN JOINT, AND A POPPING SOUND WHEN SHE WALKS. ALSO ALLEGED IS ELEVATED METAL IONS.

Description of Event or Problem · 1

ASR REVISION.ASR XL - RIGHT HIP.REASON FOR REVISION: PAIN.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
282568 ASR UNI FEMORAL IMPL SIZE 45 TOTAL HIP REPLACEMENT KWA DEPUY INTL., LTD. - 8010379 2850173

Patients

Seq Age Sex Outcome Treatment
1 70 YR Other| R