VERITY
Received Aug 30, 2021 · Event occurred Jul 30, 2021
Report 3007208013-2021-00023 · MDR key 12384231
Device
Product problems
- Break
Patient
Not reported
- No Clinical Signs, Symptoms or Conditions
- No Clinical Signs, Symptoms or Conditions
Narrative
Additional Manufacturer Narrative
UPON RECEIVING THE RETURNED DEVICE, IT WAS CONFIRMED THAT THE DEVICE WAS WITHIN CONFORMANCE FOR MATERIAL AND HARDNESS. THIS PARTICULAR CUSTOMER HAS REPORTED MULTIPLE ISSUES FOR BOTH WELL USED DEVICES AND BRAND NEW DEVICES. BASED ON THE AMOUNT OF ISSUES THIS CUSTOMER IS HAVING WITH THIS PRODUCT, IT CAN BE DETERMINED THAT SOMETHING IS OCCURRING DURING THE USE OF THE PRODUCT THAT IS CAUSING THEM TO BREAK. IF EXCESSIVE FORCE IS APPLIED TO THE TIP OF THE INSTRUMENT DAMAGE CAN OCCUR. (B)(4). THIS IS THE ONLY CUSTOMER THAT HAS REPORTED AN ISSUE WITH THE PRODUCT CODE THAT IS NEW. ALL OTHER COMPLAINTS THAT HAVE BEEN RECEIVED WERE AGED DEVICES. NO FURTHER ACTIONS ARE REQUIRED AT THIS TIME. THIS CAN BE SEEN AS THE INITIAL AND FINAL REPORT. IF ADDITIONAL INFORMATION IS OBTAINED THAT ALLEGES IN ADDITIONAL PATIENT INVOLVEMENT OR THE NEED FOR CORRECTIVE ACTIONS, A FOLLOW UP REPORT WILL BE SUBMITTED.
Description of Event or Problem
THE TIP OF THE NERVE HOOK BROKE OFF DURING A TOTAL DISC. THE PIECE FELL INTO THE PATIENT AND WAS REMOVED WITH NO HARM TO THE PATIENT.
Remedial action
- Replace