PRISMAFLEX TPE 107144

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a health professional report with the FDA on 2016-04-20 for PRISMAFLEX TPE 107144 manufactured by Gambro Industries.

Event Text Entries

[43125696] Unknown
Patient Sequence No: 1, Text Type: N, H10


[43125697] A patient in (b)(6) with encephalomyelitis was undergoing her 31st therapeutic plasma exchange (tpe) treatment. Approximately 2 minutes after the treatment started, the patient developed sudden back pain and nausea. The patient was treated with paracetamol, tramadol and metoclopramide; the treatment was discontinued without returning the blood in the extracorporeal circuit and restarted an hour later.
Patient Sequence No: 1, Text Type: D, B5


MAUDE Entry Details

Report Number8010182-2016-00027
MDR Report Key5590781
Report SourceHEALTH PROFESSIONAL
Date Received2016-04-20
Date of Report2016-04-20
Date of Event2016-01-25
Date Mfgr Received2016-03-21
Device Manufacturer Date2015-11-30
Date Added to Maude2016-04-20
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 ContactTHIERRY PALKOVICS
Manufacturer Street7 AVENUE LIONEL TERRAY
Manufacturer CityMEYZIEU
Manufacturer CountryFR
Manufacturer Phone472452525
Single Use3
Previous Use Code3
Event Type3
Type of Report3

Device Details

Brand NamePRISMAFLEX TPE
Product CodeMDP
Date Received2016-04-20
Model Number107144
Lot Number15K3003
Device Expiration Date2018-11-01
OperatorHEALTH PROFESSIONAL
Device AvailabilityN
Device Eval'ed by MfgrR
Device Sequence No1
Device Event Key0
ManufacturerGAMBRO INDUSTRIES
Manufacturer Address7 AVENUE LIONEL TERRAY MEYZIEU 69883 FR 69883


Patients

Patient NumberTreatmentOutcomeDate
101. Required No Informationntervention 2016-04-20

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