3100 HIGH FREQUENCY OSCILLATING VENTILATOR (HFOV) 3100 B 770155

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a health professional,user faci report with the FDA on 2020-03-03 for 3100 HIGH FREQUENCY OSCILLATING VENTILATOR (HFOV) 3100 B 770155 manufactured by Vyaire Medical..

Event Text Entries

[184319784] (b)(4) field service rep (fsr) evaluation: a vyaire field service representative (fsr) evaluated the device onsite. They found no power and they installed new power module. The fsr did a 7 year module adjustments. The field service representative confirmed the ventilator is ready to be used on a patient.
Patient Sequence No: 1, Text Type: N, H10


[184319785] The customer reported to vyaire medical that the 3100 b pressurizes and does not start. There is no patient involvement on the event.
Patient Sequence No: 1, Text Type: D, B5


MAUDE Entry Details

Report Number2021710-2020-11467
MDR Report Key9782877
Report SourceHEALTH PROFESSIONAL,USER FACI
Date Received2020-03-03
Date of Report2020-02-05
Date of Event2020-02-05
Date Mfgr Received2020-02-05
Device Manufacturer Date2012-07-12
Date Added to Maude2020-03-03
Event Key0
Report Source CodeManufacturer report
Manufacturer LinkY
Number of Patients in Event0
Adverse Event Flag3
Product Problem Flag3
Reprocessed and Reused Flag3
Reporter OccupationOTHER HEALTH CARE PROFESSIONAL
Health Professional3
Initial Report to FDA3
Report to FDA3
Event Location3
Manufacturer ContactMINDY FABER
Manufacturer Street26125 N. RIVERWOODS BLVD.
Manufacturer CityMETTAWA, IL
Manufacturer CountryUS
Manufacturer Phone7570116
Manufacturer G1VYAIRE MEDICAL INC.
Manufacturer Street1100 BIRD CENTER DRIVE
Manufacturer CityPALM SPRINGS, CA
Manufacturer CountryUS
Single Use3
Previous Use Code3
Event Type3
Type of Report3

Device Details

Brand Name3100 HIGH FREQUENCY OSCILLATING VENTILATOR (HFOV)
Generic NameVENTILATOR, HIGH FREQUENCY
Product CodeLSZ
Date Received2020-03-03
Model Number3100 B
Catalog Number770155
OperatorHEALTH PROFESSIONAL
Device AvailabilityY
Device Eval'ed by MfgrY
Device Sequence No1
Device Event Key0
ManufacturerVYAIRE MEDICAL.
Manufacturer Address26125 N. RIVERWOODS BLVD. METTAWA, IL US


Patients

Patient NumberTreatmentOutcomeDate
10 2020-03-03

© 2024 FDA.report
This site is not affiliated with or endorsed by the FDA.