PNEUPAC PARAPAC VENTILATOR 120003?

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a user facility report with the FDA on 2020-02-21 for PNEUPAC PARAPAC VENTILATOR 120003? manufactured by Smiths Medical Asd, Inc..

Event Text Entries

[180517708] Information was received that the o2 valve on a smiths medical pneupac parapac ventilator is not responding when plugged into oxygen/dropped possib. No patient involvement.
Patient Sequence No: 1, Text Type: D, B5


MAUDE Entry Details

Report Number3012307300-2020-01415
MDR Report Key9742489
Report SourceUSER FACILITY
Date Received2020-02-21
Date of Report2020-02-21
Date Mfgr Received2020-01-27
Device Manufacturer Date2005-09-21
Date Added to Maude2020-02-21
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 FDA3
Event Location3
Manufacturer ContactDAVE HALVERSON
Manufacturer Street6000 NATHAN LANE NORTH
Manufacturer CityMINNEAPOLIS, MN
Manufacturer CountryUS
Manufacturer G1SMITHS MEDICAL, INTERNATIONAL LTD.
Manufacturer StreetBRAMINGHAM BUSINESS PARK, ENTERPRISE WAY,
Manufacturer CityLUTON,
Manufacturer CountryUK
Single Use3
Previous Use Code3
Event Type3
Type of Report3

Device Details

Brand NamePNEUPAC PARAPAC VENTILATOR
Generic NameVENTILATOR, EMERGENCY, POWERED (RESUSCITATOR) PRODUCT CODE: BTL
Product CodeBTL
Date Received2020-02-21
Returned To Mfg2020-01-27
Model Number120003?
Catalog Number120003?
Device AvailabilityR
Device Eval'ed by MfgrN
Device Sequence No1
Device Event Key0
ManufacturerSMITHS MEDICAL ASD, INC.
Manufacturer Address6000 NATHAN LANE NORTH MINNEAPOLIS, MN US


Patients

Patient NumberTreatmentOutcomeDate
10 2020-02-21

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