FDA Adverse Event Injury Summary report: N

DEPUY DUOFIX MBT TRAY SZ 3

MDR report key: 3905113 · Received July 1, 2014

Report

Report Number
1818910-2014-22383
Event Type
Injury
Date Received
July 1, 2014
Date of Event
January 15, 2014
Report Date
June 26, 2014
Manufacturer
DEPUY IRELAND-9616671
Product Code
NJL
PMA / PMN Number
PP830055
Adverse Event
Yes
Report Source
Manufacturer report
Reporter Location
US
Reporter Occupation
PHYSICIAN

Narratives

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

Additional Manufacturer Narrative · 1

THE LCS DUOFIX FEMORAL COMPONENTS WERE VOLUNTARILY RECALLED FROM THE MARKET IN JULY 2009, AND THE LCS DUOFIX FEMORAL PRODUCT CODES ARE NOW CONSIDERED INACTIVE. FURTHER INSPECTION OF COMPONENTS WILL NOT BE PERFORMED AS THE INVESTIGATION REGARDING THE ROOT CAUSE(S) AND/OR CORRECTIVE ACTIONS ARE CONTROLLED UNDER (B)(4). WHERE INDIVIDUAL RETRIEVAL ANALYSIS IS UNDERTAKEN TO CONFIRM THE PRESENCE OF ALUMINA IN THE POLY BEARING SURFACE THEN THESE REVIEWS WILL BE ATTACHED TO THE COMPLAINT RECORD ON RECEIPT OF THE APPROVED DOCUMENT.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.

Description of Event or Problem · 1

PATIENT PRESENTED WITH PAIN AND SWELLING. UPON REVIEW, IT WAS DETERMINED THE LCS WAS A PART OF THE RECALL.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
384641 DEPUY DUOFIX MBT TRAY SZ 3 KNEE TIBIAL TRAY NJL DEPUY IRELAND-9616671 1926317

Patients

Seq Age Sex Outcome Treatment
1 Required Intervention