MIAMI J COLLAR MJ-400

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a consumer report with the FDA on 2016-04-12 for MIAMI J COLLAR MJ-400 manufactured by Ossur.

Event Text Entries

[42433376] Patient wearing spinal collar developed a rash after 2 days use post surgery. Patient had makes claims of hives, itchy and inflamed area near the collar that spread throughout. Patient discontinued use of the collar and was prescribed a medication to control the reaction and was given a soft brace to wear.
Patient Sequence No: 1, Text Type: D, B5


[45816876]
Patient Sequence No: 1, Text Type: N, H10


[45816877] Patient wearing spinal collar developed a rash after 2 days use post surgery. Patient had makes claims of hives, itchy and inflamed area near the collar that spread throughout. Patient discontinued use of the collar and was prescribed a medication to control the reaction and was given a soft brace to wear.
Patient Sequence No: 1, Text Type: D, B5


MAUDE Entry Details

Report Number3008523132-2016-00001
MDR Report Key5570635
Report SourceCONSUMER
Date Received2016-04-12
Date of Report2016-04-12
Date of Event2016-01-28
Date Mfgr Received2016-03-10
Date Added to Maude2016-04-12
Event Key0
Report Source CodeManufacturer report
Manufacturer LinkY
Number of Patients in Event0
Adverse Event Flag3
Product Problem Flag3
Reprocessed and Reused Flag3
Reporter OccupationPATIENT
Health Professional3
Initial Report to FDA3
Report to FDA3
Event Location3
Manufacturer ContactMRS. KAREN MONTES
Manufacturer Street27051 TOWNE CENTRE DRIVE
Manufacturer CityFOOTHILL RANCH CA 92610
Manufacturer CountryUS
Manufacturer Postal92610
Manufacturer Phone9493823741
Manufacturer G1OSSUR
Manufacturer StreetBLVD HECTOR TERAN TERAN 2102 EDIFICIO #1, COL. DE CANON DEL
Manufacturer CityTIJUANA, BAJA CALIFORNIA 2102
Manufacturer CountryMX
Manufacturer Postal Code2102
Single Use3
Previous Use Code3
Event Type3
Type of Report3

Device Details

Brand NameMIAMI J COLLAR
Generic NameORTHOSIS, CERVICAL
Product CodeIQK
Date Received2016-04-12
Catalog NumberMJ-400
OperatorHEALTH PROFESSIONAL
Device AvailabilityN
Device AgeDA
Device Eval'ed by MfgrR
Device Sequence No1
Device Event Key0
ManufacturerOSSUR
Manufacturer AddressBLVD HECTOR TERAN TERAN 2102 EDIFICIO #1, COL. DE CANON DEL TIJUANA, BAJA CALIFORNIA 2102 MX 2102


Patients

Patient NumberTreatmentOutcomeDate
101. Other; 2. Required No Informationntervention 2016-04-12

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