FDA Adverse Event Malfunction Summary report: N

HIGH FLOW INSUFFLATION UNIT

MDR report key: 8502268 · Received April 10, 2019

Report

Report Number
8010047-2019-01645
Event Type
Malfunction
Date Received
April 10, 2019
Date of Event
November 4, 2016
Report Date
March 9, 2020
Manufacturer
OLYMPUS MEDICAL SYSTEMS CORP.
Product Code
HIF
UDI-DI
04953170140297
PMA / PMN Number
K014166
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
CH
Reporter Occupation
OTHER

Narratives

Additional Manufacturer Narrative · 0

THIS IS A SUPPLEMENTAL REPORT TO PROVIDE ADDITIONAL INFORMATION. THE SUBJECT DEVICE WAS NOT RETURNED TO OLYMPUS MEDICAL SYSTEMS CORP. (OMSC). THE USER DID NOT PROVIDED FURTHER INFORMATION ABOUT THIS EVENT. THE DEVICE HISTORY RECORD WAS REVIEWED AND FOUND NO IRREGULARITIES. THE EXACT CAUSE OF THE REPORTED EVENT COULD NOT BE CONCLUSIVELY DETERMINED.

Additional Manufacturer Narrative · 1

THE SUBJECT UHI-4 WAS NOT RETURNED TO OLYMPUS MEDICAL SYSTEMS CORP. (OMSC). OMSC WILL INVESTIGATE THE SUBJECT UHI-4 TO IDENTIFY THE ROOT CAUSE OF THIS FAILURE PHENOMENON WHEN OMSC RECEIVES IT. THE UHI-3 INSTRUCTION MANUAL STATES THE CORRESPONDING METHOD WHEN THERE IS AN ABNORMALITY FOR THE DEVICE. THERE WERE NO FURTHER DETAILS PROVIDED. IF SIGNIFICANT ADDITIONAL INFORMATION IS RECEIVED, THIS REPORT WILL BE SUPPLEMENTED.

Description of Event or Problem · 1

(B)(6) INFORMED OLYMPUS (B)(4) OF THE EVENT BELOW ON MARCH 13TH, 2019. ON (B)(6) 2016, THE SUBJECT UHI-3 WAS USED FOR THE LAPAROSCOPIC APPENDECTOMY. AT THE END OF THE PROCEDURE, THE SUBJECT UHI-3 SHOWED A HIGH PRESSURE ALARM. THE USER REPLACED THE SUBJECT UHI-3 WITH ANOTHER DEVICE AND COMPLETED THE PROCEDURE. THE PROCEDURE DELAYED ABOUT 10 MINUTES, BUT THERE WAS NO REPORT OF THE PATIENT¿S INJURY REGARDING THIS EVENT.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
292680 HIGH FLOW INSUFFLATION UNIT HIGH FLOW INSUFFLATION UNIT HIF OLYMPUS MEDICAL SYSTEMS CORP. UHI-3 04953170140297

Patients

Seq Age Sex Outcome Treatment
1 9 YR