FDA Adverse Event Malfunction Summary report: N

GAS MODULE III RESPIRATION GAS MONITOR

MDR report key: 3091741 · Received April 30, 2013

Report

Report Number
2221819-2013-00725
Event Type
Malfunction
Date Received
April 30, 2013
Date of Event
January 15, 2013
Report Date
April 30, 2013
Manufacturer
MINDRAY DS USA, INC.
Product Code
BZK
PMA / PMN Number
062754
Report Source
Manufacturer report
Reporter Location
DE, US
Reporter Occupation
UNKNOWN

Narratives

Additional Manufacturer Narrative · 1

MINDRAY SERVICE REP REPLACED THE GAS BENCH AND VERIFIED OPERATION.

Description of Event or Problem · 1

CUSTOMER REPORTED AN ISSUE WITH THE O2 MONITORING ON THE GAS MODULE III. NO PATIENT INJURY WAS REPORTED.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
187808 GAS MODULE III RESPIRATION GAS MONITOR GAS MODULE BZK MINDRAY DS USA, INC.

Patients

Seq Age Sex Outcome Treatment
1