COMFORT COOL THUMB CMC RESTRICTION SPLINT NC79557

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed with the FDA on 2017-10-26 for COMFORT COOL THUMB CMC RESTRICTION SPLINT NC79557 manufactured by North Ccoast Medical, Inc..

Event Text Entries

[90391672] North coast medical became aware of this issue on (b)(4) 2017 from a report by: (b)(6) of (b)(6). This was after (b)(4) of (b)(4) sent (b)(4) an incident report investigation scheme, file reference: (b)(4). After learning of this incident north coast medical, inc. Performed a material test on a sample hand splint (patient did not return the original unit), and the tests conclusion was "pass".
Patient Sequence No: 1, Text Type: N, H10


[90391673] Patient experienced an allergic reaction to velcro.
Patient Sequence No: 1, Text Type: D, B5


MAUDE Entry Details

Report Number1000124207-2017-00006
MDR Report Key6982132
Date Received2017-10-26
Date of Report2017-10-11
Date of Event2016-08-25
Date Mfgr Received2017-07-20
Date Added to Maude2017-10-26
Event Key0
Report Source CodeManufacturer report
Manufacturer LinkY
Number of Patients in Event0
Adverse Event Flag3
Product Problem Flag3
Reprocessed and Reused Flag3
Reporter OccupationMEDICAL EQUIPMENT COMPANY TECHNICIAN/REPRESENTATIVE
Health Professional3
Initial Report to FDA3
Report to FDA3
Event Location3
Manufacturer ContactMR. RUSSELL MACDERMOTT
Manufacturer Street8100 CAMINO ARROYO
Manufacturer CityGILROY 95020
Manufacturer CountryUS
Manufacturer Postal95020
Manufacturer Phone4087765000
Manufacturer G1NORHT COAST MEDICAL, INC.
Manufacturer Street8100 CAMINO ARROYO
Manufacturer CityGILROY CA 95020
Manufacturer CountryUS
Manufacturer Postal Code95020
Single Use3
Previous Use Code3
Event Type3
Type of Report0

Device Details

Brand NameCOMFORT COOL THUMB CMC RESTRICTION SPLINT
Generic NameCOMFORT COOL
Product CodeILH
Date Received2017-10-26
Model NumberNC79557
Catalog NumberNC79557
Lot NumberN/A
OperatorLAY USER/PATIENT
Device AvailabilityN
Device Eval'ed by MfgrR
Device Sequence No1
Device Event Key0
ManufacturerNORTH CCOAST MEDICAL, INC.
Manufacturer Address8100 CAMINO ARROYO GILROY CA 95020 US 95020


Patients

Patient NumberTreatmentOutcomeDate
101. Other 2017-10-26

© 2024 FDA.report
This site is not affiliated with or endorsed by the FDA.