MCOMPASS BIOFEEDBACK 2-CHANNEL CATHETER RMD-002-004

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed with the FDA on 2019-03-06 for MCOMPASS BIOFEEDBACK 2-CHANNEL CATHETER RMD-002-004 manufactured by Medspira Llc.

Event Text Entries

[137973579] During biofeedback session, balloon part of the biofeedback catheter broke while in the patient. Manufacturer response for anorectal manometry catheter, mcompass biofeedback 2 channel anorectal manometry catheter (per site reporter). This is the fifth case of this type for this particular device experienced by (b)(6) hospitals over the past six weeks. Company has been made aware and has made arrangements to replace all existing stock with this additional lot number (see previous report). Unaware if other follow up has occurred.
Patient Sequence No: 1, Text Type: D, B5


MAUDE Entry Details

Report Number8394217
MDR Report Key8394217
Date Received2019-03-06
Date of Report2019-02-12
Date of Event2019-02-07
Report Date2019-02-18
Date Reported to FDA2019-02-18
Date Reported to Mfgr2019-03-06
Date Added to Maude2019-03-06
Event Key0
Report Source CodeUser Facility 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 Report3

Device Details

Brand NameMCOMPASS BIOFEEDBACK 2-CHANNEL CATHETER
Generic NameDEVICE, BIOFEEDBACK
Product CodeHCC
Date Received2019-03-06
Model NumberRMD-002-004
Catalog NumberRMD-002-004
Lot Number19011401
OperatorHEALTH PROFESSIONAL
Device Availability*
Device Eval'ed by Mfgr*
Device Sequence No1
Device Event Key0
ManufacturerMEDSPIRA LLC
Manufacturer Address2718 SUMMER STREET NE MINNEAPOLIS MN 55413 US 55413


Patients

Patient NumberTreatmentOutcomeDate
101. Other 2019-03-06

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