FDA Adverse Event Malfunction Summary report: N

FIREBIRD SFS

MDR report key: 20955466 · Received December 17, 2024

Report

Report Number
2183449-2024-00026
Event Type
Malfunction
Date Received
December 17, 2024
Date of Event
September 17, 2024
Report Date
January 7, 2025
Manufacturer
ORTHOFIX US LLC
Product Code
LXH
UDI-DI
18257200045600
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
US
Reporter Occupation
PHYSICIAN
Health Professional
Yes

Narratives

Additional Manufacturer Narrative · 0

THE ROD GRIPPER (PN:51-1480 LN:39802-PE09) WAS RETURNED FOR INVESTIGATION AND SENT TO THE MOR FOR EVALUATION. FA FROM GAUTHIER: THE PIN (SCREW) SET CLOSEST TO THE JAWS. THAT CAME OFF IN THE FIELD, WAS NOT RETURNED WITH THE PART. WHEN A NEW SET OF PINS WAS USED TO REPLACE THE MISSING PAIR, THE ROD GRIPPER WAS TESTED AND WOULD FUNCTION PROPERLY. THE 3 SETS OF PINS ON THE PART WERE CHECKED FOR ADHESIVE STRENGTH. THE 1ST SET CLOSEST TO THE TEETH WOULD READILY UNTHREAD WITH SLIGHT EFFORT. THE 2ND SET OF PINS WOULD EASILY UNTHREAD WHEN CHECKED. THE 3RD SET OF PINS WAS STILL SECURELY HELD TOGETHER WITH ADHESIVE. WITH SOME SIGNIFICANT EFFORT, THESE WERE ALSO ABLE TO BE UNTHREADED. THE THREADS WERE CHECKED ON ALL 3 SETS AND THE 1ST AND 2ND SET CLOSEST TO THE TEETH HAD DRIED BUT ADEQUATE ADHESIVE OBSERVED ON THE THREADS, AND THE 3RD SET STILL HAD DRIED BUT SIGNIFICANT ADHESIVE ON THE THREADS. AS THE PIN SET THAT CAME LOOSE WAS NOT RETURNED. THE THREADS ON THOSE PINS WERE NOT ABLE TO BE CHECKED FOR ADEQUATE ADHESIVE. THE ADHESIVE ON THE 3 CHECKED SETS HAD WORN OUT MOST LIKELY DUE TO SIGNIFICANT STERILIZATION/DRYING CYCLES OVER THE 11 YEARS OF PART USAGE. THE TEETH ON THE GRIPPER WERE ALSO CHECKED AND FOUND TO BE WORN ON THEIR SIDE EDGES, WHERE SOME MATERIAL WAS FOUND TO BE ROLLED OVER THE ENDS, FROM USAGE. SOME WEAR ON THE COMPONENTS WAS OBSERVED BETWEEN THE MOVING PARTS OF THE ROD GRIPPER. THE LASER MARKING ON THE PART WAS OBSERVED TO BE WORN FROM USAGE OVER TIME. THE ROD GRIPPER HAS MOST LIKELY SEEN SIGNIFICANT USE I NUMBER OF STERILIZATIONS AS THE PART IS OVER 11 YEARS OLD . THE ROOT CAUSE OF THE PIN SET THAT UNTHREADED AND CAME OFF THE ROD GRIPPER WAS MOST LIKELY DUE TO THE NUMBER OF STERILIZATION/DRYING CYCLES CAUSING THE ADHESIVE TO WEAR OUT OVER THE YEARS OF SERVICE, ALLOWING FOR THE PINS TO UNTHREAD AND COME OFF THE INSTRUMENT. THE DHR WAS REVIEWED FOR THIS ORDER AND THERE WERE NO NONCONFORMANCE FOUND THAT WOULD HAVE CONTRIBUTED TO THIS COMPLAINT. THE WO (B)(4) PART FOR THIS COMPLAINT WAS RETURNED TO GAUTHIER ON 12-19-2024. THE PIN( SCREW) SET CLOSEST TO THE JAWS. THAT CAME OFF IN THE FIELD, WAS NOT RETURNED WITH THE PART. THIS PART ORIGINALLY SHIPPED FROM GAUTHIER IN MAY 2013, AND HAS MOST LIKELY BEEN IN THE FIELD FOR OVER 11 YEARS. THE INSTRUMENT HAD MINIMAL WEAR MARKS FROM USAGE OVER THE YEARS. THE P/N # 51 -1480 AND LOT # 39802-PE09 WERE LASER MARKED ON THE PART AND WERE WORN FROM USAGE.

Additional Manufacturer Narrative · 0

PRODUCT HAS RETURNED FOR INVESTIGATION BUT THE INVESTIGATION IS NOT COMPLETE. A SUPPLEMENTAL REPORT WILL BE COMPLECTED ONCE THE INVESTIGATION IS DONE.

Description of Event or Problem · 0

IT WAS REPORTED THAT DURING A SCOLIOSIS SURGERY, THE SCREW OF THE GRIPPER MOVED OUT OF PLACE. SURGERY WAS COMPLETED WITH ANOTHER ROD GRIPPER THAT WAS INSIDE OF THE TRAY WITH NO ADVERSE EFFECTS TO THE PATIENT. REPORTING FOR A ONE HOUR TIME DELAY IN SURGERY.

Description of Event or Problem · 0

IT WAS REPORTED THAT DURING A SCOLIOSIS SURGERY, THE SCREW OF THE GRIPPER MOVED OUT OF PLACE. SURGERY WAS COMPLETED WITH ANOTHER ROD GRIPPER THAT WAS INSIDE OF THE TRAY WITH NO ADVERSE EFFECTS TO THE PATIENT. REPORTING FOR A ONE HOUR TIME DELAY IN SURGERY.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
238870 FIREBIRD SFS ROD GRIPPER LXH ORTHOFIX US LLC 51-1480 39802-PE09 18257200045600

Patients

Seq Age Sex Outcome Treatment
1 NA Unknown Other