CUNITI WIRE 205-1903

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 2016-12-02 for CUNITI WIRE 205-1903 manufactured by Ormco Corporation.

Event Text Entries

[61398630] It was alleged that a patient had swallowed a 2cm piece of arch wire. Wire has been replaced and no long term consequences can be foreseen.
Patient Sequence No: 1, Text Type: N, H10


[61398631] Patient swallowed 2cm of wire.
Patient Sequence No: 1, Text Type: D, B5


MAUDE Entry Details

Report Number2016150-2016-00006
MDR Report Key6142518
Report SourceHEALTH PROFESSIONAL
Date Received2016-12-02
Date of Report2016-11-09
Date of Event2016-10-29
Date Mfgr Received2016-11-09
Date Added to Maude2016-12-02
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 ContactMRS. SUZETTE RAMPAIR-JOHNSON
Manufacturer Street1332 SOUTH LONE HILL AVE.
Manufacturer CityGLENDORA CA 91740
Manufacturer CountryUS
Manufacturer Postal91740
Manufacturer Phone9099625730
Manufacturer G1ORMCO CORPORATION
Manufacturer Street1332 SOUTH LONE HILL AVE.
Manufacturer CityGLENDORA CA 91740
Manufacturer CountryUS
Manufacturer Postal Code91740
Single Use3
Previous Use Code3
Event Type3
Type of Report3

Device Details

Brand NameCUNITI WIRE
Generic NameCOPPER NITI WIRE
Product CodeDZC
Date Received2016-12-02
Catalog Number205-1903
Lot Number16A8A
Device AvailabilityN
Device Eval'ed by MfgrR
Device Sequence No1
Device Event Key0
ManufacturerORMCO CORPORATION
Manufacturer Address1332 SOUTH LONE HILL AVE. GLENDORA CA 91740 US 91740


Patients

Patient NumberTreatmentOutcomeDate
101. Other 2016-12-02

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