PNEUPAC? PARAPAC PLUS 310 P310NUS

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a distributor report with the FDA on 2020-03-11 for PNEUPAC? PARAPAC PLUS 310 P310NUS manufactured by Smiths Medical Asd; Inc..

Event Text Entries

[183087053] Information was received indicating that the gauge to a smiths medical pneupac? Parapac plus was reported to intermittently be working properly. There were no reported adverse effects.
Patient Sequence No: 1, Text Type: D, B5


MAUDE Entry Details

Report Number3012307300-2020-01875
MDR Report Key9821032
Report SourceDISTRIBUTOR
Date Received2020-03-11
Date of Report2020-03-11
Date Mfgr Received2020-02-12
Device Manufacturer Date2019-04-09
Date Added to Maude2020-03-11
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 N
Manufacturer CityMINNEAPOLIS,, MN
Manufacturer CountryUS
Manufacturer Phone3833310
Manufacturer G1SMITHS MEDICAL ASD; INC.
Manufacturer Street6000 NATHAN LANE N
Manufacturer CityMINNEAPOLIS,, MN
Manufacturer CountryUS
Single Use3
Previous Use Code3
Event Type3
Type of Report3

Device Details

Brand NamePNEUPAC? PARAPAC PLUS
Generic NameVENTILATOR, EMERGENCY, POWERED (RESUSCITATOR)
Product CodeBTL
Date Received2020-03-11
Returned To Mfg2020-02-19
Model Number310
Catalog NumberP310NUS
Lot Number1903095
Device AvailabilityR
Device Eval'ed by MfgrN
Device Sequence No1
Device Event Key0
ManufacturerSMITHS MEDICAL ASD; INC.
Manufacturer Address6000 NATHAN LANE N MINNEAPOLIS,, MN US


Patients

Patient NumberTreatmentOutcomeDate
10 2020-03-11

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