VECTORTAS MINI SCREW

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a other report with the FDA on 2016-09-19 for VECTORTAS MINI SCREW manufactured by Ormco Corporation.

Event Text Entries

[55041226] It was alleged that a patient had and allergic reaction; no medical prescriptions required. It was confirmed no serious injury was associated with this incident. The patient is doing fine.
Patient Sequence No: 1, Text Type: N, H10


[55041227] It was alleged that a patient had an allergic reaction to vectortas screws.
Patient Sequence No: 1, Text Type: D, B5


MAUDE Entry Details

Report Number2016150-2016-00004
MDR Report Key5960034
Report SourceOTHER
Date Received2016-09-19
Date of Report2016-09-02
Date Added to Maude2016-09-19
Event Key0
Report Source CodeManufacturer report
Manufacturer LinkY
Number of Patients in Event0
Adverse Event Flag3
Product Problem Flag3
Reprocessed and Reused Flag3
Health Professional0
Initial Report to FDA0
Report to FDA3
Event Location3
Manufacturer ContactMRS. SUZETTE RAMPAIR-JOHNSON
Manufacturer Street1332 SOUTH LONE HILL AVENUE
Manufacturer CityGLENDORA CA 91740
Manufacturer CountryUS
Manufacturer Postal91740
Manufacturer Phone9099625730
Manufacturer G1ORMCO CORPORATION
Manufacturer Street1332 SOUTH LONE HILL AVENUE
Manufacturer CityGLENDORA CA 91740
Manufacturer CountryUS
Manufacturer Postal Code91740
Single Use3
Previous Use Code3
Event Type3
Type of Report3

Device Details

Brand NameVECTORTAS MINI SCREW
Generic NameVECTORTAS MINI SCREW
Product CodeOAT
Date Received2016-09-19
Device AvailabilityN
Device Eval'ed by MfgrR
Device Sequence No1
Device Event Key0
ManufacturerORMCO CORPORATION
Manufacturer Address1332 SOUTH LONE HILL AVENUE GLENDORA CA 91740 US 91740


Patients

Patient NumberTreatmentOutcomeDate
101. Other 2016-09-19

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