FDA Adverse Event Malfunction Summary report: N

MIC* TJ FEEDING TUBE KIT 18 FR, 45CM (ENDO/RADIOL)

MDR report key: 4975078 · Received August 5, 2015

Report

Report Number
9611594-2015-00132
Event Type
Malfunction
Date Received
August 5, 2015
Date of Event
July 22, 2015
Report Date
September 17, 2015
Manufacturer
HALYARD HEALTH
Product Code
KGC
PMA / PMN Number
PK080253
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
NY, US
Reporter Occupation
OTHER HEALTH CARE PROFESSIONAL

Narratives

Additional Manufacturer Narrative · 1

UDI # UNKNOWN. THE DEVICE HISTORY RECORD FOR THE REPORTED LOT NUMBER, AA4230N12, WAS REVIEWED AND DOCUMENTED THAT THE LOT WAS MANUFACTURED ACCORDING TO THE APPROVED MANUFACTURING PROCEDURES, SPECIFICATIONS, AND THEN RELEASED BY QUALITY ASSURANCE. 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 COMPLAINT (B)(4).

Additional Manufacturer Narrative · 1

(B)(4). UPON COMPLETION OF THE INVESTIGATION; A FOLLOW-UP REPORT WILL BE FILED. 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 COMPLAINT (B)(4). DEVICE NOT RETURNED.

Description of Event or Problem · 1

IT WAS REPORTED THAT THE TRANSJEJUNAL FEEDING TUBE INITIALLY PLACED ON (B)(6) 2015 DEVELOPED A TEAR DOWN THE JEJUNAL PORTION OF THE TUBE. THE TRANSJEJUNAL TUBE WAS REPLACED WITHOUT FURTHER INCIDENT. NO PATIENT INJURY REPORTED.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
517042 MIC* TJ FEEDING TUBE KIT 18 FR, 45CM (ENDO/RADIOL) DH EF BALLOON TUBES PRODUCTS KGC HALYARD HEALTH 0250-18 AA4230N12

Patients

Seq Age Sex Outcome Treatment
1 85 YR