RAPID PALATAL EXPANDER

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a 05 report with the FDA on 2012-10-01 for RAPID PALATAL EXPANDER manufactured by Allesee Orthodontic Appliances.

Event Text Entries

[2906195] A doctor alleged that a patient experienced a tongue ulceration while wearing the rapid palatal expander appliance.
Patient Sequence No: 1, Text Type: D, B5


[10143566] The doctor removed the appliance and the patient was prescribed a chlorhexidine rinse for treatment. A new expansion appliance with a more streamlined design will be fabricated with consideration for patient comfort. To date, the patient is doing fine and has fully recovered.
Patient Sequence No: 1, Text Type: N, H10


MAUDE Entry Details

Report Number2184045-2012-00008
MDR Report Key2767425
Report Source05
Date Received2012-10-01
Date of Report2012-09-06
Date of Event2012-07-25
Date Mfgr Received2012-09-06
Date Added to Maude2012-10-01
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 FDA0
Event Location0
Manufacturer ContactMRS. WENDY GARMAN
Manufacturer Street1717 W COLLINS AVE
Manufacturer CityORANGE CA 92867
Manufacturer CountryUS
Manufacturer Postal92867
Manufacturer Phone7145167602
Manufacturer G1ALLESEE ORTHODONTIC APPLIANCES
Manufacturer Street13931 SPRING STREET
Manufacturer CitySTURTEVANT WI 53177
Manufacturer CountryUS
Manufacturer Postal Code53177
Single Use3
Previous Use Code3
Event Type3
Type of Report3

Device Details

Brand NameRAPID PALATAL EXPANDER
Generic NameRETAINER, SCREW EXPANSION, ORTHODONTIC
Product CodeDYJ
Date Received2012-10-01
ID NumberW/O # 7378542
OperatorOTHER
Device AvailabilityN
Device Eval'ed by MfgrR
Device Sequence No1
Device Event Key0
ManufacturerALLESEE ORTHODONTIC APPLIANCES
Manufacturer Address13931 SPRING STREET STURTEVANT WI 53177 US 53177


Patients

Patient NumberTreatmentOutcomeDate
101. Other; 2. Required No Informationntervention 2012-10-01

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