FDA Adverse Event Malfunction Summary report: N

MAQUET HL-20 INTEGRATED PERFUSION SYSTEM

MDR report key: 5520849 · Received March 23, 2016

Report

Report Number
8010762-2016-00212
Event Type
Malfunction
Date Received
March 23, 2016
Date of Event
March 16, 2016
Report Date
March 16, 2016
Manufacturer
MAQUET CARDIOPULMONARY AG
Product Code
DTQ
PMA / PMN Number
K943803
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
NY
Reporter Occupation
OTHER HEALTH CARE PROFESSIONAL

Narratives

Additional Manufacturer Narrative · 1

UPDATE 03/23/2016 01:45 PM (B)(4): MAQUET MEDICAL SYSTEMS, USA SUBMITS THIS REPORT ON BEHALF OF THE LEGAL MANUFACTURER OF THE DEVICE MAQUET CARDIOPULMONARY (B)(4). A MAQUET SERVICE TECHNICIAN WILL INVESTIGATE THE UNIT. A SUPPLEMENTAL MEDWATCH WILL BE SUBMITTED WHEN ADDITIONAL INFORMATION BECOMES AVAILABLE.

Additional Manufacturer Narrative · 1

THE ISSUE HAS BEEN REEVALUATED WITH THE RESULT THAT THIS ISSUE "EPROM ERROR ON HL20" IS NOT REPORTABLE. AS THE EPROM ERROR IS PART OF THE SELF TEST OF THE HL20, WHICH IS ALWAYS PERFORMED PRIOR TO USE (DURING STARTUP OF THE DEVICE, AND THE EPROM IS NOT TESTED AT ANY LATER POINT IN TIME, IT CAN BE EXCLUDED THAT THE ERROR WILL OCCUR DURING PATIENT TREATMENT. ADDITIONAL BASED ON THE TREND SEARCH ANALYSIS NO COMPLAINT WAS FOUND WITH THE MENTIONED ISSUE HAPPENED DURING PATIENT TREATMENT. ALL REPORTED ISSUES OCCURRED PRIOR TO USE.

Description of Event or Problem · 1

UPDATE 03/23/2016 01:06 PM (B)(4):CUSTOMER STATED THAT BEFORE USE/PROCEDURE THE LOANER WOULD DISPLAY A EPROM ERROR AT POWER UP. (B)(4).

Description of Event or Problem · 1

(B)(4).

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
176882 MAQUET HL-20 INTEGRATED PERFUSION SYSTEM CONSOLE, HEART-LUNG MACHINE, CARDIOPULMONARY BYPASS DTQ MAQUET CARDIOPULMONARY AG MCP00703239

Patients

Seq Age Sex Outcome Treatment
1