FDA Adverse Event Malfunction Summary report: N

MIC-KEY LOW - PROFILE JEJUNAL FEEDING TUBE

MDR report key: 7110353 · Received December 12, 2017

Report

Report Number
9611594-2017-00164
Event Type
Malfunction
Date Received
December 12, 2017
Report Date
November 15, 2017
Manufacturer
HALYARD HEALTH
Product Code
KNT
PMA / PMN Number
UNKNOWN
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
CA
Reporter Occupation
OTHER

Narratives

Additional Manufacturer Narrative · 1

THE ACTUAL COMPLAINT PRODUCT WAS NOT RETURNED FOR EVALUATION. A REVIEW OF THE DEVICE HISTORY RECORD IS NOT POSSIBLE AS NO LOT NUMBER WAS PROVIDED. ROOT CAUSE COULD NOT BE DETERMINED. ALL INFORMATION REASONABLY KNOWN AS OF 07-DEC-2017 HAS BEEN INCLUDED IN THIS HEALTH AUTHORITY REPORT. SHOULD ADDITIONAL INFORMATION BE OBTAINED, A FOLLOW-UP HEALTH AUTHORITY REPORT WILL BE PROVIDED. THE INFORMATION PROVIDED BY HALYARD HEALTH REPRESENTS ALL OF THE KNOWN INFORMATION AT THIS TIME. DESPITE GOOD FAITH EFFORTS TO OBTAIN ADDITIONAL INFORMATION, THE COMPLAINANT / REPORTER WAS UNABLE OR UNWILLING TO PROVIDE ANY FURTHER PATIENT, PRODUCT, OR PROCEDURAL DETAILS TO HALYARD HEALTH. HALYARD HEALTH HAS NO INDEPENDENT KNOWLEDGE OF THE EVENT REPORTED BUT IS RELAYING THE INFORMATION THAT WAS PROVIDED BY THE USER FACILITY WHERE THE INCIDENT OCCURRED. THIS PRODUCT INCIDENT IS DOCUMENTED IN THE HALYARD HEALTH COMPLAINT DATABASE AND IDENTIFIED AS (B)(4). DEVICE NOT RETURNED.

Description of Event or Problem · 1

IT WAS REPORTED IN THE PUBLICATION THAT "OUR INSTITUTION GENERALLY USED THE MICKEY GJT (HALYARD HEALTH; (B)(4))" AND THERE WAS AN INCIDENT OF "MAJOR COMPLICATIONS. COMPLICATIONS OF GJT WITH SIGNIFICANT MORBIDITY OR MORTALITY: INTUSSUSCEPTION..." IT IS CURRENTLY UNKNOWN WHICH PRODUCTS CONTRIBUTED TO THE EVENTS AND, THEREFORE, THIS REPORT IS BEING SUBMITTED OUT OF AN ABUNDANCE OF CAUTION.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
889268 MIC-KEY LOW - PROFILE JEJUNAL FEEDING TUBE UNKNOWN KNT HALYARD HEALTH UNKNOWN UNKNOWN

Patients

Seq Age Sex Outcome Treatment
1