FDA Adverse Event Injury Summary report: N

SMARTSETMV ENDURANCE 20 G

MDR report key: 2121374 · Received June 1, 2011

Report

Report Number
1818910-2011-08623
Event Type
Injury
Date Received
June 1, 2011
Date of Event
April 4, 2011
Report Date
May 6, 2011
Manufacturer
DEPUY CMW
Product Code
LOD
PMA / PMN Number
P960001/S005
Removal / Correction Number
NA
Adverse Event
Yes
Report Source
Manufacturer report
Reporter Location
IT
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. THE RETAINED SAMPLES WERE CONDITIONED AND TESTED AT AN AMBIENT TEMPERATURE OF 23 DEG C. ALL HANDLING AND MECHANICAL STRENGTH RESULTS WERE REVIEWED AND THEY ARE ALL WITHIN SPECIFICATION. A REVIEW OF DEVICE HISTORY RECORDS FINDS NO MANUFACTURING DEVIATIONS OR ANOMALIES THAT WOULD HAVE CONTRIBUTED TO THE EVENT. A REVIEW OF MICRO AND STERILITY TESTS FINDS NO DEVIATIONS OR ANOMALIES THAT WOULD HAVE CONTRIBUTED TO THE EVENT. THE INVESTIGATION COULD NOT VERIFY OR IDENTIFY ANY PRODUCT CONTRIBUTION TO THE REPORTED EVENT WITH THE INFORMATION PROVIDED. BASED ON THE INVESTIGATION, THE NEED FOR CORRECTIVE ACTION IS NOT INDICATED. DEPUY CONSIDERS THE INVESTIGATION CLOSED AT THIS TIME. SHOULD THE PRODUCT AND/OR ADDITIONAL INFORMATION BE RECEIVED, THE INVESTIGATION WILL BE RE-OPENED.

Description of Event or Problem · 1

THE SURGEON CLAIMS THAT THE CEMENT USED DID NOT PERFECTLY ADHERE WITH THE IMPLANT DEVICES. IT RATHER REMAINED STUCK ON THE DEVICES THEMSELVES.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1 SMARTSETMV ENDURANCE 20 G 87 LOD LOD DEPUY CMW NA 2526053

Patients

Seq Age Sex Outcome Treatment
1 NA Required Intervention