FDA Adverse Event Malfunction Summary report: N

R-PILOT, 6X, STERILE

MDR report key: 19457349 · Received June 4, 2024

Report

Report Number
9611053-2024-00098
Event Type
Malfunction
Date Received
June 4, 2024
Report Date
July 30, 2024
Manufacturer
VDW GMBH
Product Code
EKS
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
GM
Reporter Occupation
DENTIST
Health Professional
Yes

Narratives

Additional Manufacturer Narrative · 0

SIX R-PILOT FILES 25MM WERE RETURNED (ONE FILE IN LOOSE + FIVE UNUSED FILES). THE FILE IN LOOSE IS BROKEN IN THE ACTIVE PART (FATIGUE). NO MATERIAL DEFECT WAS FOUND DURING ANALYSIS OF THE RUPTURE PATTERN. NOTHING UNUSUAL TO REPORT WAS FOUND DURING DHRS REVIEW (BATCHES #1832596 AND #1832274). UNUSED FILES WERE EVALUATED AND WERE FOUND IN COMPLIANCE WITH SPECIFICATIONS. ROOT CAUSES ARE NOT IDENTIFIED. WE WILL TRACK THIS KIND OF EVENT AND MONITOR THE TREND. ROOT CAUSES ARE NOT IDENTIFIED. ALL COMPLAINTS ARE MONITORED THROUGH THE MONTHLY PRODUCT SURVEILLANCE COMMITTEE AND A CORRECTIVE ACTION COULD BE DETERMINED BY THE COMMITTEE.

Additional Manufacturer Narrative · 0

AS A RESULT OF THIS MALFUNCTION, THE POTENTIAL FOR SURGICAL INTERVENTION EXISTS TO PRECLUDE PERMANENT DAMAGE TO A BODY STRUCTURE OR PERMANENT IMPAIRMENT OF A BODY FUNCTION AS EVIDENCED BY PREVIOUS REPORTED EVENTS WITH SIMILAR FILES. THIS EVENT, THEREFORE, IS REPORTABLE PER 21CFR PART 803. THE DEVICE IS AVAILABLE FOR EVALUATION, THOUGH HAS NOT BEEN RETURNED AS OF THIS REPORT. EVALUATION RESULTS WILL BE SUBMITTED AS THEY BECOME AVAILABLE.

Description of Event or Problem · 0

IN THIS EVENT IT IS REPORTED THAT R-PILOT, 6X, STERILE BROKE DURING USE. THE BROKEN PART COULD NOT BE RETRIEVED AND WAS INCORPORATED INTO THE FILLING. NO INJURY.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
174562 R-PILOT, 6X, STERILE FILE, PULP CANAL, ENDODONTIC EKS VDW GMBH 435792

Patients

Seq Age Sex Outcome Treatment
1 NA Unknown