FDA Adverse Event Injury Summary report: N

HEATER-COOLER SYSTEM 3T

MDR report key: 7521207 · Received May 17, 2018

Report

Report Number
9611109-2018-00965
Event Type
Injury
Date Received
May 17, 2018
Date of Event
May 6, 2014
Report Date
May 17, 2018
Manufacturer
LIVANOVA DEUTSCHLAND
Product Code
DWC
Removal / Correction Number
Z-2076/2081-2015
Adverse Event
Yes
Report Source
Manufacturer report
Reporter Location
SZ
Reporter Occupation
HEALTH PROFESSIONAL

Narratives

Additional Manufacturer Narrative · 1

SERIAL NUMBER IS UNKNOWN. THIS INFORMATION WILL BE PROVIDED IN A SUPPLEMENTAL REPORT IF MADE AVAILABLE. THE HEATER-COOLER 16-02-80 IS NOT DISTRIBUTED IN THE USA, BUT IT IS SIMILAR TO HEATER-COOLER 16-02-85, WHICH IS DISTRIBUTED IN THE USA (510(K) NUMBER: K052601). AS THE SERIAL NUMBER IS UNKNOWN, THE DEVICE MANUFACTURE DATE COULD NOT BE DETERMINED. THIS INFORMATION WILL BE PROVIDED IN A SUPPLEMENTAL REPORT IF MADE AVAILABLE. LIVANOVA (B)(4) IMPLEMENTED A FIELD SAFETY NOTICE FOR DISINFECTION AND CLEANING OF HEATER-COOLER DEVICES. THE Z NUMBER IS Z-2076/2081-2015. LIVANOVA (B)(4) MANUFACTURES THE HEATER-COOLER SYSTEM 3T. THE INCIDENT OCCURRED IN (B)(6). THROUGH FURTHER COMMUNICATION LIVANOVA (B)(4) LEARNED THAT THE FACILITY WILL NOT RELEASE ANY FURTHER INFORMATION. CORRECTIVE ACTIONS ARE IN PROGRESS FOR THIS ISSUE. IF ANY ADDITIONAL INFORMATION PERTINENT TO THE REPORTED EVENT IS RECEIVED, IT WILL BE PROVIDED IN A SUPPLEMENTAL REPORT. DEVICE NOT RETURNED.

Description of Event or Problem · 1

LIVANOVA (B)(4) RECEIVED A REPORT THAT A PATIENT WHO UNDERWENT A SURGERY ON (B)(6) 2014 WAS FOUND TO BE INFECTED WITH MYCABTERIUM CHIMAREA. IT WAS REPORTED THAT A HEATER-COOLER SYSTEM WAS USED DURING THE PROCEDURE.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
365373 HEATER-COOLER SYSTEM 3T CONTROLLER, TEMPERATURE, CARDIOPULMONARY BYPASS DWC LIVANOVA DEUTSCHLAND 16-02-80

Patients

Seq Age Sex Outcome Treatment
1