FDA Adverse Event Malfunction Summary report: N

POLYAXIAL SCREW DRIVER

MDR report key: 3492514 · Received October 25, 2013

Report

Report Number
2032593-2013-00068
Event Type
Malfunction
Date Received
October 25, 2013
Date of Event
October 1, 2013
Report Date
October 25, 2013
Manufacturer
SEASPINE, INC.
Product Code
HXX
Report Source
Manufacturer report
Reporter Location
NC, US
Reporter Occupation
OTHER

Narratives

Additional Manufacturer Narrative · 1

THE DEVICE INVOLVED IN THE REPORTED INCIDENT HAS BEEN RECEIVED FOR EVALUATION. AN INVESTIGATION HAS BEEN INITIATED BASED ON THE REPORTED INFO.

Description of Event or Problem · 1

THIS IS THE FIRST OF THREE REPORTS CONCERNING THE SAME PT AND SAME SURGERY. THIS REPORT CONCERNS A MALIBU POLYAXIAL SCREWDRIVER. (PRODUCT ID 91-2110). IT WAS REPORTED DURING A POSTERIOR LUMBAR INTERBODY FUSION (PLIF) SURGERY, THE MALIBU POLYAXIAL SCREWDRIVER STRIPPED. THERE WAS A 10 TO 15 MINUTE DELAY IN SURGERY DUE TO THE REPORTED ISSUES. THERE WAS NO REPORTED INJURY TO THE PT.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
549478 POLYAXIAL SCREW DRIVER MALIBU HXX SEASPINE, INC. AL552404F

Patients

Seq Age Sex Outcome Treatment
1 59 YR