FDA Adverse Event Injury Summary report: N

DXTEND STAND PE CUP D38 +6MM

MDR report key: 1972496 · Received January 26, 2011

Report

Report Number
1818910-2011-00586
Event Type
Injury
Date Received
January 26, 2011
Date of Event
December 27, 2010
Report Date
December 27, 2010
Manufacturer
DEPUY FRANCE S.A.
Product Code
HSD
PMA / PMN Number
K062250
Removal / Correction Number
NA
Adverse Event
Yes
Report Source
Manufacturer report
Reporter Location
AS
Reporter Occupation
OTHER

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.

Additional Manufacturer Narrative · 1

THE DEVICES ASSOCIATED WITH THIS REPORT WERE NOT RETURNED. A SEARCH OF THE COMPLAINT DATABASE FOUND NO PRIOR REPORTS FOR BOTH OF THE REPORTED PART AND LOT NUMBER COMBINATIONS. A DEPUY FRANCE SUPPLIER REVIEWED THE DEVICE HISTORY RECORDS AND FOUND THE PRODUCTS CONFORMED TO THE REQUIRED SPECIFICATIONS AND FOUND NO MANUFACTURING DEVIATIONS OR ANOMALIES. BASED ON THE INVESTIGATION THE NEED FOR CORRECTIVE ACTION IS NOT INDICATED. DEPUY CONSIDERS THE INVESTIGATION CLOSED. SHOULD ANY ADDITIONAL INFORMATION BE RECEIVED TO CHANGE THE OUTCOME OF THE PERFORMED INVESTIGATION, THE COMPLAINT WILL BE RE-OPENED.

Description of Event or Problem · 1

PT PRESENTED TO HOSP WITH PAIN AND SWELLING TO SHOULDER. FOLLOWING INVESTIGATIONS, PT DIAGNOSED WITH DEEP TISSUE INFECTION AND PRESCRIBED INTRAVENOUS ANTIBIOTICS. INITIALLY PERFORMED A WOUND WASHOUT WITH LITTLE IMPROVEMENT. ON (B)(6) 2010 - DEVICE EXCHANGE. INFECTED MEMBRANE REMOVED FROM THE UNDERSIDE OF BOTH IMPLANTS AND SENT FOR PATHOLOGY, RESULTS PENDING. THERE WAS NO EVIDENCE OF LOOSE COMPONENTS AS THE TIME OF REVISION SURGERY.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1 DXTEND STAND PE CUP D38 +6MM 87HSD 87KWS HSD DEPUY FRANCE S.A. NA 5020715

Patients

Seq Age Sex Outcome Treatment
1 67 YR Required Intervention