FDA Adverse Event Malfunction Summary report: N

AIRWAY MOBILESCOPE

MDR report key: 20281517 · Received September 23, 2024

Report

Report Number
9610595-2024-19001
Event Type
Malfunction
Date Received
September 23, 2024
Report Date
October 9, 2024
Manufacturer
AIZU OLYMPUS CO., LTD.
Product Code
EOQ
UDI-DI
04953170407260
PMA / PMN Number
K201300
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
JA
Reporter Occupation
003

Narratives

Additional Manufacturer Narrative · 0

THE DEVICE EVALUATION IS ONGOING. SHOULD ADDITIONAL RELEVANT INFORMATION BECOME AVAILABLE, A SUPPLEMENTAL REPORT WILL BE SUBMITTED.

Additional Manufacturer Narrative · 0

THIS REPORT IS BEING SUPPLEMENTED TO PROVIDE ADDITIONAL INFORMATION BASED ON THE LEGAL MANUFACTURER'S FINAL INVESTIGATION. A REVIEW OF THE DEVICE HISTORY RECORD FOUND NO DEVIATIONS THAT COULD HAVE CAUSED OR CONTRIBUTED TO THE REPORTED ISSUE. BASED ON THE RESULTS OF THE INVESTIGATION, A DEFINITIVE ROOT CAUSE OF THE OBSERVED IMAGE GUIDE HOSE COATING PEELING COULD NOT BE DETERMINED, HOWEVER, THE ISSUE WAS LIKELY THE RESULT OF REPETITIVE USE STRESS, EXTERNAL FACTORS AND OF USER HANDLING/MISHANDLING. THE EVENT MAY BE DETECTED/PREVENTED BY FOLLOWING THE INSTRUCTIONS FOR USE SECTIONS BELOW: MAF-DM2, MAF-GM2 CHAPTER 3: PREPARATION AND INSPECTION_3.6 INSPECTING THE ENDOSCOPE. MAF-TM2 INSTRUCTION MANUAL OPERATION SECTION. OLYMPUS WILL CONTINUE TO MONITOR FIELD PERFORMANCE FOR THIS DEVICE.

Description of Event or Problem · 0

IT WAS OBSERVED DURING THE DEVICE INSPECTION, THAT THE COATING OF THE IMAGE GUIDE HOSE OF THE AIRWAY MOBILESCOPE HAD PEELED OFF. THERE WERE NO REPORTS OF PATIENT INVOLVEMENT.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1503518 AIRWAY MOBILESCOPE AIRWAY MOBILESCOPE EOQ AIZU OLYMPUS CO., LTD. MAF-DM2 04953170407260

Patients

Seq Age Sex Outcome Treatment
1 NA Unknown