HERBST

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 2012-03-16 for HERBST manufactured by Allesee Orthodontic Appliances.

Event Text Entries

[15212109] The customer stated that the ul band of the herbst appliance was cutting into the patient's cheeks.
Patient Sequence No: 1, Text Type: D, B5


[15754052] The patient was prescribed chlorhexidine, an antiseptic rinse, for treatment. Patient is doing fine and has fully recovered. The axle casing on the upper appliance will be repositioned with consideration to patient comfort.
Patient Sequence No: 1, Text Type: N, H10


MAUDE Entry Details

Report Number2184045-2012-00005
MDR Report Key2494923
Report Source05
Date Received2012-03-16
Date of Report2012-02-15
Date Mfgr Received2012-02-15
Device Manufacturer Date2012-01-15
Date Added to Maude2012-03-19
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 FDA0
Event Location0
Manufacturer ContactMR. ORLANDO TADEO, JR.
Manufacturer Street1717 W COLLINS AVE
Manufacturer CityORANGE CA 92867
Manufacturer CountryUS
Manufacturer Postal92867
Manufacturer Phone7145167419
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 NameHERBST
Generic NameBITE-JUMPING ORTHODONTIC APPLIANCE
Product CodeEJF
Date Received2012-03-16
ID NumberWORK ORDER #34391298
OperatorOTHER
Device AvailabilityY
Device Eval'ed by MfgrN
Device Sequence No1
Device Event Key0
ManufacturerALLESEE ORTHODONTIC APPLIANCES
Manufacturer Address13931 SPRING STREET STURTEVANT WI 53177 US 53177


Patients

Patient NumberTreatmentOutcomeDate
101. Other 2012-03-16

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