PORTLESS TUBING

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed with the FDA on 2018-05-11 for PORTLESS TUBING manufactured by Unk.

Event Text Entries

[108292942] Coring occurred with portless tubing after being spiked.
Patient Sequence No: 1, Text Type: D, B5


MAUDE Entry Details

Report NumberMW5077204
MDR Report Key7511837
Date Received2018-05-11
Date of Report2018-05-09
Date of Event2018-05-09
Date Added to Maude2018-05-14
Event Key0
Report Source CodeVoluntary report
Manufacturer LinkN
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
Single Use3
Previous Use Code3
Event Type3
Type of Report0

Device Details

Brand NamePORTLESS TUBING
Generic NameTUBING, FLUID DELIVERY
Product CodeFPK
Date Received2018-05-11
Device AvailabilityN
Device Eval'ed by MfgrI
Device Sequence No1
Device Event Key0
ManufacturerUNK
Manufacturer AddressUNK UNK


Patients

Patient NumberTreatmentOutcomeDate
101. Other 2018-05-11

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