BIRD HIGH FLOW BLENDER SERIES 03800B

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a distributor,foreign report with the FDA on 2018-04-26 for BIRD HIGH FLOW BLENDER SERIES 03800B manufactured by Vyaire Medical, Inc.

Event Text Entries

[106644122] Vyaire file identification: (b)(4). Any additional information received from the customer will be included in a follow-up report. At this time, vyaire has not received the suspect device for evaluation.
Patient Sequence No: 1, Text Type: N, H10


[106644123] The customer reported while using the bird blender; the device has a leak between the rotameter and blender. The customer reported there is no patient involvement associated with the event.
Patient Sequence No: 1, Text Type: D, B5


[115010600]
Patient Sequence No: 1, Text Type: N, H10


MAUDE Entry Details

Report Number2021710-2018-07775
MDR Report Key7465054
Report SourceDISTRIBUTOR,FOREIGN
Date Received2018-04-26
Date of Report2018-04-30
Date of Event2018-03-30
Date Mfgr Received2018-04-30
Device Manufacturer Date2017-01-01
Date Added to Maude2018-04-26
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 ContactKRISTIN GRAF
Manufacturer Street22745 SAVI RANCH PARKWAY
Manufacturer CityYORBA LINDA CA 92887
Manufacturer CountryUS
Manufacturer Postal92887
Manufacturer G1VYAIRE MEDICAL, INC
Manufacturer Street1100 BIRD CENTER DR.
Manufacturer CityPALM SPRINGS CA 92262
Manufacturer CountryUS
Manufacturer Postal Code92262
Single Use3
Previous Use Code3
Event Type3
Type of Report3

Device Details

Brand NameBIRD HIGH FLOW BLENDER SERIES
Generic NameMIXER, BREATHING GASES, ANESTHESIA INHALATION
Product CodeBZR
Date Received2018-04-26
Model NumberBLENDER
Catalog Number03800B
OperatorHEALTH PROFESSIONAL
Device AvailabilityY
Device AgeDA
Device Eval'ed by MfgrR
Device Sequence No1
Device Event Key0
ManufacturerVYAIRE MEDICAL, INC
Manufacturer Address22745 SAVI RANCH PARKWAY YORBA LINDA CA 92887 US 92887


Patients

Patient NumberTreatmentOutcomeDate
10 2018-04-26

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