FDA Adverse Event Malfunction Summary report: N

T-PAL SPACER APPLICATOR INNER SHAFT

MDR report key: 3242753 · Received July 23, 2013

Report

Report Number
8030965-2013-04382
Event Type
Malfunction
Date Received
July 23, 2013
Date of Event
July 2, 2013
Report Date
July 2, 2013
Manufacturer
SYNTHES GMBH
Product Code
LXH
PMA / PMN Number
EXEMPT
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
FL, US
Reporter Occupation
HEALTH PROFESSIONAL

Narratives

Additional Manufacturer Narrative · 1

DEVICE IS USED FOR TREATMENT, NOT DIAGNOSIS. DEVICE HISTORY RECORDS WERE REVIEWED AND NO ISSUES WERE FOUND THAT WOULD CONTRIBUTE TO THE REPORTED CONDITION. THE INVESTIGATION

Additional Manufacturer Narrative · 1

DEVICE WAS USED FOR TREATMENT, NOT DIAGNOSIS. PLACEHOLDER.

Description of Event or Problem · 1

THIS FOLLOW UP IS BEING SENT BECAUSE OF A FACILITY MEDWATCH RECEIVED. THE FACILITY MEDWATCH WILL BE ATTACHED ALONG WITH THIS MEDWATCH, AND ANY INFORMATION FROM THE FACILITY MEDWATCH WILL NOT BE REPEATED IN THIS MEDWATCH.

Description of Event or Problem · 1

IT WAS REPORTED T-PAL SPACER APPLICATOR WAS USED FOR THE INTERBODY CAGE DURING THE PROCEDURE. THE T-PAL APPLICATOR WOULD NOT RELEASE FROM THE CAGE ONCE IMPLANTED. WHEN THE SURGEON WAS ABLE TO REMOVE THE APPLICATOR THE FORK PORTION OF THE APPLICATOR WAS OBSERVED TO BE DEFORMED. THE CAGE WAS IMPLANTED IN THE CANAL AND THE SURGEON IMMEDIATELY TRIED TO REMOVE THE CAGE. THE CAGE CAME OUT BROKEN. THE SURGEON REPORTED DAMAGE TO THE PATIENTS SPINAL CORD. THE SURGEON BELIEVES THE PATIENT WILL BE PARAPLEGIC. THIS REPORT IS FOR THE T-PAL SPACER APPLICATOR INNER SHAFT. THIS REPORT IS 3 OF 4 FOR COMPLAINT (B)(4).

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
343332 T-PAL SPACER APPLICATOR INNER SHAFT LXH SYNTHES GMBH 8247716

Patients

Seq Age Sex Outcome Treatment
1