PULSION PICCO MONITORING KIT PV8115

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed with the FDA on 2018-09-28 for PULSION PICCO MONITORING KIT PV8115 manufactured by Pulsion Medical Systems Se.

Event Text Entries

[122195432] Further information has been requested and investigation is ongoing. A supplemental medwatch report will be sent when the investigation is completed. (b)(4). (b)(6).
Patient Sequence No: 1, Text Type: N, H10


[122195433] It was reported that upon set up of a picco monitoring kit the connection line to the patient was leaking. No harm to the patient occurred. Manufacturer reference #: (b)(4).
Patient Sequence No: 1, Text Type: D, B5


MAUDE Entry Details

Report Number3003263092-2018-00010
MDR Report Key7919126
Date Received2018-09-28
Date of Report2018-11-30
Date of Event2018-08-29
Date Mfgr Received2018-09-14
Date Added to Maude2018-09-28
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 FDA3
Event Location3
Manufacturer StreetMAQUET CRITICAL CARE AB R
Manufacturer CitySOLNA
Manufacturer CountrySW
Manufacturer Phone0498945991
Manufacturer G1MAGNUS LINDQVIST
Manufacturer StreetMAQUET CRITICAL CARE AB R
Manufacturer CitySOLNA
Manufacturer CountrySW
Single Use3
Previous Use Code3
Event Type3
Type of Report0

Device Details

Brand NamePULSION PICCO MONITORING KIT
Generic NamePROBE, THERMODILUTION
Product CodeKRB
Date Received2018-09-28
Returned To Mfg2018-11-06
Catalog NumberPV8115
OperatorHEALTH PROFESSIONAL
Device AvailabilityR
Device AgeDA
Device Eval'ed by MfgrN
Device Sequence No1
Device Event Key0
ManufacturerPULSION MEDICAL SYSTEMS SE
Manufacturer AddressPULSION MEDICAL SYSTEMS SE HANS-RIEDL-STR. 21 85622 FELDKIRCHEN GM


Patients

Patient NumberTreatmentOutcomeDate
10 2018-09-28

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