FDA Adverse Event Malfunction Summary report: N

XVISION SPINE SYSTEM (XVS)

MDR report key: 17377667 · Received July 24, 2023

Report

Report Number
3016571711-2023-00005
Event Type
Malfunction
Date Received
July 24, 2023
Date of Event
June 27, 2023
Report Date
July 24, 2023
Manufacturer
AUGMEDICS LTD.
Product Code
OLO
UDI-DI
07290113780231
PMA / PMN Number
K211188
Adverse Event
Yes
Report Source
Manufacturer report
Reporter Location
IS
Reporter Occupation
PHYSICIAN
Health Professional
Yes

Narratives

Description of Event or Problem · 0

SURGERY: REMOVAL OF HARDWARE L2-L5, NEW SCREWS PLACED WITH XVISION FROM T9-S1. DURING INSTRUMENTATION, A NAVLOCK TOOL ADAPTOR WAS DETACHED FROM THE GEARSHIFT TOOL THAT WAS FIXATED ON IT. VISUAL INSPECTION OF THE ADAPTER REVEALED THAT THE ADAPTER WAS DAMAGED. A NEW ADAPTER WAS PLACED ONTO THE GEARSHIFT TOOL AND THE PROCEDURE WAS COMPLETED WITH NO FURTHER ISSUES. POST-OPERATIVELY, ONE OF THE STAINLESS-STEEL BALLS OF THE ADAPTERS WAS FOUND IN A STERILE AREA, NEAR THE OTHER TOOLS. AN O-ARM SPIN AND FLAT PANEL X-RAY WERE PERFORMED, AND THE SURGEON AND TEAM DID NOT SEE ANY OTHER BALLS WITHIN THE PATIENT'S BODY. AS A RESULT, ALL SITE NAVLOCK ADAPTORS WERE INSPECTED, AND 8 WERE FOUND DAMAGED WITH MISSING ONE, OR TWO, BALLS AND BROKEN PEEK. THE ADAPTERS ARE MANUFACTURED FROM WELL-KNOWN USED MATERIALS IN MEDICAL DEVICES. ALL 9 DAMAGED ADAPTERS WERE QUARANTINED AT THE SITE. FOUR ADDITIONAL ADAPTORS AT THE SITE WERE FOUND TO BE UNDAMAGED. THE COMPANY TRIED TO REPRODUCE THE EVENT USING SIMILAR TOOLS AND ADAPTORS FOLLOWING A SIMILAR CLINICAL WORKFLOW OF THE SURGEON WITH NO SUCCESS. A MALFUNCTION DURING THE MANUFACTURING PROCESS WAS ALSO RULED OUT, AS WELL AS A DAMAGED BATCH. ALL OTHER ADAPTERS WERE VISUALLY INSPECTED AT ALL OTHER SITES AND FOUND TO BE UNDAMAGED. WHILE THE INVESTIGATION IS CONTINUING, AT THIS POINT IT INCREASINGLY APPEARS THAT THIS EVENT IS ISOLATED TO THE (B)(6) HOSPITAL. ACCORDING TO 21 CFR 803, MDR IS NOT REQUIRED SINCE MALFUNCTION WAS ASSESSED NOT TO CAUSE A SERIOUS INJURY. YET, THE COMPANY DECIDED TO REPORT THIS EVENT.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
771090 XVISION SPINE SYSTEM (XVS) XVISION SPINE SYSTEM (XVS) OLO AUGMEDICS LTD. NAVIGATED TOOL ADAPTOR NA 07290113780231

Patients

Seq Age Sex Outcome Treatment
1 Unknown Other