FDA Adverse Event Malfunction Summary report: N

NUVASIVE PRECEPT SPINAL SYSTEM

MDR report key: 15211061 · Received August 11, 2022

Report

Report Number
2031966-2022-00144
Event Type
Malfunction
Date Received
August 11, 2022
Report Date
August 11, 2022
Manufacturer
NUVASIVE, INCORPORATED
Product Code
MAX
UDI-DI
00887517484505
PMA / PMN Number
K171894
Removal / Correction Number
NA
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
TH
Reporter Occupation
PHYSICIAN
Health Professional
Yes

Narratives

Additional Manufacturer Narrative · 0

THE DEVICE WAS RETURNED AND THE COMPLAINT WAS CONFIRMED AS THE TIP WAS FOUND TO BE FRACTURED. THE DEVICE EVALUATION DETERMINED THE FRACTURE PATTERN TO BE CAUSED BY EXCESSIVE, OFF-ANGLED FORCE. ADDITIONALLY, A DHR REVIEW OF THE REPORTED DEVICE IDENTIFIED IT HAS BEEN IN THE FIELD FOR OVER 10 YEARS. TORQUE HANDLE INFORMATION WAS NOT PROVIDED. IT IS UNKNOWN WHETHER THE SURGEON UTILIZED A TORQUE HANDLE OR A FREEHAND TECHNIQUE. BASED ON THE INFORMATION PROVIDED THE ROOT CAUSE WAS DETERMINED TO BE A COMBINATION OF WEAR FATIGUE AND EXCESSIVE, OFF-ANGLED EXCESSIVE FORCE. NO ADDITIONAL INVESTIGATION CAN BE COMPLETED. LABELING REVIEW: "...PATIENT EDUCATION: PREOPERATIVE INSTRUCTIONS TO THE PATIENT ARE ESSENTIAL. THE PATIENT SHOULD BE MADE AWARE OF THE POTENTIAL RISKS OF THE SURGERY..." "...DO NOT IMPLANT THE INSTRUMENTS: COMPLICATIONS TO THE PATIENT MAY INCLUDE, BUT ARE NOT LIMITED TO: BREAKAGE OF THE DEVICE, WHICH COULD MAKE NECESSARY REMOVAL DIFFICULT OR SOMETIMES IMPOSSIBLE, WITH POSSIBLE CONSEQUENCES OF LATE INFECTION AND MIGRATION. BREAKAGE COULD CAUSE INJURY TO THE PATIENT..." "...PRE-OPERATIVE WARNINGS: THE METHOD OF USE FOR THE INSTRUMENTS ARE TO BE DETERMINED BY THE USER¿S EXPERIENCE AND TRAINING IN SURGICAL PROCEDURES. THE INSTRUMENTS SHOULD BE TREATED AS ANY PRECISION INSTRUMENT AND SHOULD BE CAREFULLY PLACED ON TRAYS, CLEANED AFTER EACH USE, AND STORED, ACCORDING TO GENERALLY ACCEPTED HOSPITAL METHODS AND PRACTICES. THE INSTRUMENTS SHOULD BE CAREFULLY EXAMINED PRIOR TO USE FOR FUNCTIONALITY, EXCESSIVE WEAR, OR DAMAGE. A DAMAGED INSTRUMENT SHOULD NOT BE USED AS THIS MAY INCREASE THE RISK OF MALFUNCTION AND POTENTIAL PATIENT INJURY. CARE SHOULD BE USED DURING SURGICAL PROCEDURES TO PREVENT DAMAGE TO THE DEVICES AND INJURY TO THE PATIENT..." "...INTRA-OPERATIVE WARNINGS: THE PHYSICIAN SHOULD TAKE PRECAUTIONS AGAINST PUTTING UNDUE STRESS ON THE SPINAL AREA WITH INSTRUMENTS. ANY SURGICAL TECHNIQUE SHOULD BE CAREFULLY FOLLOWED. IT IS IMPORTANT THAT THE SURGEON EXERCISE EXTREME CAUTION WHEN WORKING IN CLOSE PROXIMITY TO VITAL ORGANS, NERVES, OR VESSELS, AND THAT THE FORCE APPLIED TO THE INSTRUMENTATION IS NOT EXCESSIVE, TO PREVENT POTENTIAL INJURY TO THE PATIENT. OVER-BENDING, NOTCHING, STRIKING, AND/OR SCRATCHING OF IMPLANTS WITH ANY INSTRUMENT SHOULD BE AVOIDED TO REDUCE THE RISK OF BREAKAGE. WHEN USING THE MAXCESS MAS TLIF SYSTEM FOR DISTRACTION CARE MUST BE TAKEN TO AVOID DAMAGING THE PEDICLES WHICH COULD COMPROMISE PEDICLE SCREW PURCHASE. THE PHYSICAL CHARACTERISTICS REQUIRED FOR MANY INSTRUMENTS DO NOT PERMIT THEM TO BE MANUFACTURED FROM IMPLANTABLE MATERIALS. IF ANY BROKEN FRAGMENTS OF INSTRUMENTS REMAIN IN THE BODY OF A PATIENT, THEY COULD CAUSE ALLERGIC REACTIONS OR INFECTIONS. IF AN INSTRUMENT BREAKS IN SURGERY AND FRAGMENTS GO INTO THE PATIENT, THESE PIECES SHOULD BE REMOVED PRIOR TO CLOSURE AND SHOULD NOT BE IMPLANTED..."

Description of Event or Problem · 0

DURING A SPINAL PROCEDURE ON AN UNKNOWN DATE, THE TIP FRACTURED OFF WHILE DRIVING THE SCREW AND WAS LEFT IN-SITU. NO PATIENT HARM WAS REPORTED AS A RESULT OF THE REPORTED EVENT.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1945104 NUVASIVE PRECEPT SPINAL SYSTEM THORACOLUMBOSACRAL PEDICLE SCREW SYSTEM MAX NUVASIVE, INCORPORATED 7459014 EM3227 00887517484505

Patients

Seq Age Sex Outcome Treatment
1 Prefer Not To Disclose