FDA Adverse Event Injury Summary report: N

UNKNOWN DEPUY PINNACLE HIP LINER

MDR report key: 3201160 · Received July 2, 2013

Report

Report Number
1818910-2013-20349
Event Type
Injury
Date Received
July 2, 2013
Date of Event
April 30, 2013
Report Date
June 3, 2013
Manufacturer
8010379 DEPUY INTL., LTD.
Product Code
KWA
Adverse Event
Yes
Report Source
Manufacturer report
Reporter Location
US
Reporter Occupation
PATIENT

Narratives

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. THE DEVICES ASSOCIATED WITH THIS REPORT WERE NOT RETURNED. REVIEW OF THE DEVICE HISTORY RECORDS AND/OR A COMPLAINT DATABASE SEARCH WAS NOT POSSIBLE AS THE PRODUCT AND LOT CODES REQUIRED WERE NOT PROVIDED. THE INVESTIGATION COULD NOT DRAW ANY CONCLUSIONS REGARDING THE REPORTED EVENT WITH THE INFORMATION AVAILABLE. BASED ON THE INABILITY TO IDENTIFY A ROOT CAUSE, THE NEED FOR CORRECTIVE ACTION WAS NOT INDICATED. DEPUY CONSIDERS THE INVESTIGATION CLOSED AT THIS TIME. SHOULD ADDITIONAL INFORMATION BE RECEIVED, THE INFORMATION WILL BE REVIEWED AND THE INVESTIGATION WILL BE RE-OPENED AS NECESSARY.

Additional Manufacturer Narrative · 1

THIS COMPLAINT IS STILL UNDER INVESTIGATION. DEPUY WILL NOTIFY THE FDA OF THE RESULTS OF THIS INVESTIGATION ONCE IT HAS BEEN COMPLETED.

Description of Event or Problem · 1

PATIENT CONTACTED DEPUY. MEDICAL RECORDS WERE OBTAINED. MEDICAL RECORDS INDICATE PATIENT WAS REVISED DUE TO GRAY FLUID WITHIN THE HIP JOIN WITH GRAY STAINING OF THE SYNOVIAL TISSUES. A LARGE AMOUNT OF SCAR TISSUE WAS REMOVED WITHIN THE HIP JOINT.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
301619 UNKNOWN DEPUY PINNACLE HIP LINER LINER KWA 8010379 DEPUY INTL., LTD. UNKNOWN

Patients

Seq Age Sex Outcome Treatment
1 66 YR Required Intervention