HUDSON OSMO PLUS 800-10

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a 05,06,07 report with the FDA on 2010-08-26 for HUDSON OSMO PLUS 800-10 manufactured by Teleflex Medical.

Event Text Entries

[20215651] The event is reported as: the osmo unit would not pass he leak test on the ventilator.
Patient Sequence No: 1, Text Type: D, B5


[20579905] The device sample was returned for evaluation. The results of the evaluation are not available at the time of this report.
Patient Sequence No: 1, Text Type: N, H10


MAUDE Entry Details

Report Number3004365956-2010-00200
MDR Report Key1829199
Report Source05,06,07
Date Received2010-08-26
Date of Report2010-08-10
Date of Event2010-08-09
Date Mfgr Received2010-08-10
Date Added to Maude2010-12-28
Event Key0
Report Source CodeManufacturer report
Manufacturer LinkY
Number of Patients in Event0
Adverse Event Flag3
Product Problem Flag3
Reprocessed and Reused Flag3
Health Professional3
Initial Report to FDA3
Report to FDA0
Event Location0
Manufacturer ContactMICHAEL TAGGART, VP
Manufacturer StreetP.O. BOX 12600
Manufacturer CityRTP NC 27709
Manufacturer CountryUS
Manufacturer Postal27709
Manufacturer Phone9194334916
Manufacturer G1TELEFLEX MEDICAL
Manufacturer StreetAVE. TRANSORMACION 5954 PARQUE INDUSTRIAL FINSA
Manufacturer CityNUEVO LAREDO 88275
Manufacturer CountryMX
Manufacturer Postal Code88275
Single Use3
Remedial ActionOT
Previous Use Code3
Removal Correction NumberNA
Event Type3
Type of Report3

Device Details

Brand NameHUDSON OSMO PLUS
Generic NameWATER TRAP
Product CodeBYH
Date Received2010-08-26
Model NumberNA
Catalog Number800-10
Lot Number02H0902332
ID NumberNA
OperatorOTHER
Device AvailabilityY
Device AgeDA
Device Eval'ed by MfgrY
Device Sequence No1
Device Event Key0
ManufacturerTELEFLEX MEDICAL
Manufacturer AddressNUEVO LAREDO MX


Patients

Patient NumberTreatmentOutcomeDate
10 2010-08-26

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