FDA Adverse Event Malfunction Summary report: N

SERVO-I

MDR report key: 8055327 · Received November 9, 2018

Report

Report Number
8010042-2018-00600
Event Type
Malfunction
Date Received
November 9, 2018
Date of Event
October 7, 2018
Report Date
December 4, 2018
Manufacturer
MAQUET CRITICAL CARE AB
Product Code
CBK
PMA / PMN Number
K123149
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
WI
Reporter Occupation
BIOMEDICAL ENGINEER

Narratives

Additional Manufacturer Narrative · 0

GETINGE USA SALES, LLC (IMPORTER) IS SUBMITTING THIS REPORT ON BEHALF OF MAQUET CRITICAL CARE AB (MANUFACTURER). REF. EXEMPTION #: E2018003 GETINGE USA SALES, LLC 45 BARBOUR POND DRIVE WAYNE, NJ 07470 CONTACT PERSON: (B)(4).

Additional Manufacturer Narrative · 0

GETINGE USA SALES, LLC (IMPORTER) IS SUBMITTING THIS REPORT ON BEHALF OF MAQUET CRITICAL CARE AB (MANUFACTURER). REF. EXEMPTION #: E2018003. GETINGE USA SALES, LLC 45 BARBOUR POND DRIVE WAYNE, NJ 07470. CONTACT PERSON: (B)(4). THE USER FACILITY PERFORMS SERVICE OF THEIR VENTILATORS BY THEMSELVES AND DID NOT REQUEST ANY SERVICE. IT HAS NOT BEEN COMMUNICATED IF ANY PARTS WERE REPLACED. THE INVESTIGATION OF THE PROVIDED VENTILATOR LOGS FOUND ALARMS FOR LOW O2 CONCENTRATION. THE LOGS DO NOT CONTAIN ANY TECHNICAL ERROR CODES INDICATING ANY VENTILATOR MALFUNCTION AT THE TIME OF THE EVENT. PRE-USE CHECK WAS SUCCESSFULLY PERFORMED PRIOR VENTILATION WAS STARTED. SINCE NO PARTS WERE RETURNED FOR INVESTIGATION, THE ROOT CAUSE OF THE REPORTED ALARMS HAS NOT BEEN DETERMINED.

Description of Event or Problem · 0

IT WAS REPORTED THAT THE O2 CONCENTRATION WAS FLUCTUATING DURING PATIENT TREATMENT. THERE WAS NO PATIENT HARM. (B)(4).

Description of Event or Problem · 0

(B)(4).

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
897325 SERVO-I VENTILATOR, CONTINUOUS, FACILITY USE CBK MAQUET CRITICAL CARE AB

Patients

Seq Age Sex Outcome Treatment
1