FDA Adverse Event Malfunction Summary report: N

BOM 7MM EXTENDED LENGTH ENDOSCOPE

MDR report key: 5405539 · Received February 2, 2016

Report

Report Number
2242352-2016-00113
Event Type
Malfunction
Date Received
February 2, 2016
Report Date
January 7, 2016
Manufacturer
MAQUET CV
Product Code
GCJ
PMA / PMN Number
K014250
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
MO, US
Reporter Occupation
NURSE

Narratives

Additional Manufacturer Narrative · 1

FEB. 02, 2016 03:29 PM (GMT-5:00) ADDED BY (B)(6): THE DEVICE HAS NOT YET BEEN RETURNED TO MAQUET CARDIAC SURGERY FOR EVALUATION. WE ARE FOLLOWING UP WITH THE CUSTOMER FOR THE RETURN OF THE DEVICE. A SUPPLEMENTAL REPORT WILL BE SUBMITTED IF THE DEVICE IS RECEIVED. (B)(4).

Additional Manufacturer Narrative · 1

THIS IS A REUSABLE OEM DEVICE; THEREFORE, A LOT HISTORY REVIEW WAS NOT APPLICABLE. THE PRODUCT IS NOT RETURNING. A LOT NUMBER WAS NOT PROVIDED AND THE SPECIFIC PRODUCT SERIAL NUMBER CANNOT BE IDENTIFIED FROM A SHIP HISTORY, THEREFORE IT IS IMPOSSIBLE TO OBTAIN A CERTIFICATE OF CONFORMANCE. (B)(4).

Description of Event or Problem · 1

THE HOSPITAL REPORTED THAT DURING AN ENDOSCOPIC VEIN HARVESTING PROCEDURE, THEY COULDN'T VISUALIZE THROUGH THE BOM 7MM EXTENDED LENGTH ENDOSCOPE. A REPLACEMENT DEVICE WAS USED TO COMPLETE THE PROCEDURE. THE HOSPITAL DID NOT REPORT ANY PATIENT EFFECTS.

Description of Event or Problem · 1

THE HOSPITAL REPORTED THAT DURING AN ENDOSCOPIC VEIN HARVESTING PROCEDURE, THEY COULDN'T VISUALIZE THROUGH THE BOM 7MM EXTENDED LENGTH ENDOSCOPE. A REPLACEMENT DEVICE WAS USED TO COMPLETE THE PROCEDURE. THE HOSPITAL DID NOT REPORT ANY PATIENT EFFECTS

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
63968 BOM 7MM EXTENDED LENGTH ENDOSCOPE LAPAROSCOPE, GENERAL & PLASTIC SURGERY GCJ MAQUET CV

Patients

Seq Age Sex Outcome Treatment
1