ORTHO SOLO 740-0271

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 2017-06-19 for ORTHO SOLO 740-0271 manufactured by Ormco Corporation.

Event Text Entries

[77863822] It was alleged that a patient lost enamel to teeth. It was confirmed that no serious injury was associated with this incident. The doctor fixed the patients teeth that lost the enamel and a new device was replaced. To date the patient is doing fine.
Patient Sequence No: 1, Text Type: N, H10


[77863823] It was alleged that a patient lost enamel to teeth while using ortho solo.
Patient Sequence No: 1, Text Type: D, B5


[112066314] The product involved in the alleged incident was not returned; therefore, a retain sample was evaluated, yielding results within specifications.
Patient Sequence No: 1, Text Type: N, H10


[112066315] It was alleged that a patient lost enamel to teeth while using ortho solo.
Patient Sequence No: 1, Text Type: D, B5


MAUDE Entry Details

Report Number2016150-2017-00001
MDR Report Key6649985
Report SourceOTHER
Date Received2017-06-19
Date of Report2017-05-04
Date of Event2017-05-04
Date Mfgr Received2017-12-07
Date Added to Maude2017-06-19
Event Key0
Report Source CodeManufacturer report
Manufacturer LinkY
Number of Patients in Event0
Adverse Event Flag3
Product Problem Flag3
Reprocessed and Reused Flag3
Health 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 NameORTHO SOLO
Generic NameORTHO SOLO
Product CodeDYH
Date Received2017-06-19
Catalog Number740-0271
Device Availability*
Device AgeDA
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 2017-06-19

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