VENTILATORS PNEUPAC VENTILATORS PARAPAC VENTILATOR MEDIC PARAPAC 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 2020-02-23 for VENTILATORS PNEUPAC VENTILATORS PARAPAC VENTILATOR MEDIC PARAPAC 120003 manufactured by Smiths Medical Asd,inc.

Event Text Entries

[180519539] Information received a smiths medical ventilators
Patient Sequence No: 1, Text Type: D, B5


MAUDE Entry Details

Report Number3012307300-2020-01414
MDR Report Key9742955
Report SourceUSER FACILITY
Date Received2020-02-23
Date of Report2020-02-23
Date Mfgr Received2020-01-24
Device Manufacturer Date2006-01-26
Date Added to Maude2020-02-23
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 ContactDAVE HALVERSON
Manufacturer Street6000 LANE N
Manufacturer CityMINNEAPOLIS, MN
Manufacturer CountryUS
Manufacturer Phone3833310
Manufacturer G1SMITHS MEDICAL INTERNATIONAL LTD.,
Manufacturer StreetBRAMINGHAM BUSINESS PARK, ENTERPRISE WAY,
Manufacturer CityLUTON, BEDS, LU3 4BU
Manufacturer CountryUK
Single Use3
Previous Use Code3
Event Type3
Type of Report3

Device Details

Brand NameVENTILATORS PNEUPAC VENTILATORS PARAPAC
Generic NameVENTILATOR, EMERGENCY, POWERED (RESUSCITATOR)
Product CodeBTL
Date Received2020-02-23
Returned To Mfg2020-01-27
Model NumberVENTILATOR MEDIC PARAPAC
Catalog Number120003
Device AvailabilityR
Device Eval'ed by MfgrN
Device Sequence No1
Device Event Key0
ManufacturerSMITHS MEDICAL ASD,INC
Manufacturer Address6000 LANE N MINNEAPOLIS, MN US


Patients

Patient NumberTreatmentOutcomeDate
10 2020-02-23

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