FDA Adverse Event Injury Summary report: N

ENDURA NO-REACT DURAL SUBSTITUTE, 4 CM X 4 CM

MDR report key: 952968 · Received November 14, 2007

Report

Report Number
3003418325-2007-00017
Event Type
Injury
Date Received
November 14, 2007
Report Date
November 14, 2007
Manufacturer
SHELHIGH
Product Code
GXQ
Adverse Event
Yes
Report Source
Manufacturer report
Reporter Location
CA, US
Reporter Occupation
INVALID DATA

Narratives

Additional Manufacturer Narrative · 1

INTEGRA LIFESCIENCES CORP IS FILING A DISTRIBUTOR REPORT BASED UPON INFO PROVIDED BY THE USER FACILITY. THE MFR, SHELHIGH, INC. WILL BE NOTIFIED VIA EMAIL OF THE REPORTED COMPLAINT AND PROVIDED WITH A COPY OF THIS REPORT VIA FEDEX.

Description of Event or Problem · 1

ON 10/24/07 INTEGRA LIFESCIENCES RECEIVED A LETTER FROM THE FDA INDICATING THAT A VOLUNTARY MEDWATCH HAD BEEN FILED ON THE ENDURA DURAL GRAFT. THE MEDWATCH STATED THAT IN 05, LAMINECTOMY REDO FOR A PROGRESSIVE THORACIC MYELOPATHY, DURA PATCH GRAFT, FDA RECALL OF GRAFT SUSPECT STERILIZATION ENVIRONMENT CONTROLS FAILURE. FIFTEEN DAYS LATER, SURGERY TO REPAIR LEAK. IN 04 SURGERY TO REPAIR LEAK. ADDITIONAL INFO: INCIDENT DATE: 2005 A REVIEW OF THE COMPLAINT DATABASE FROM 10/1/04 TO PRESENT DOES NOT INDICATE THAT INTEGRA WAS AWARE OF THE INCIDENT. AN INTEGRA REP SPOKE TO THE REP FROM THE USER FACILITY ON 10/29/07 TO OBTAIN ADDITIONAL INFO AND A COPY OF THE MEDWATCH FILED. THE USER FACILITY DID NOT RETAIN A COPY OF THE MEDWATCH IN THEIR FILES. THE REP AT THE USER FACILITY STATED THAT THEY CANNOT IMPLICATE ENDURA AS THE CAUSE OF THE INCIDENT. THE MEDWATCH FILING WAS THE RESULT OF A VOLUNTARY RECALL AND NOT DUE TO THE HEALTH PROFESSIONAL OR PT REPORTING THE ADVERSE EVENT.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1 ENDURA NO-REACT DURAL SUBSTITUTE, 4 CM X 4 CM ENDURA GXQ SHELHIGH * 040212NRB

Patients

Seq Age Sex Outcome Treatment
1 Hospitalization