TRANSBOND PLUS SELF ETCHING PRIMER 712-090

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 2005-05-06 for TRANSBOND PLUS SELF ETCHING PRIMER 712-090 manufactured by 3m Unitek.

Event Text Entries

[379070] Orthodontist stated that the brackets, along with the archwire, detached from the patient's teeth because of an adhesive-bond failure which he attributed to the etchant/primer. As a result, the archwire lodged in the patient's throat. Patient was taken to an accident & emergency hospital where the archwire was removed.
Patient Sequence No: 1, Text Type: D, B5


MAUDE Entry Details

Report Number2020467-2005-00004
MDR Report Key599787
Report Source05
Date Received2005-05-06
Date of Report2005-04-27
Date of Event2005-04-01
Date Mfgr Received2005-04-27
Date Added to Maude2005-05-09
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 Location0
Manufacturer ContactMARLYN SCHEFF
Manufacturer Street2724 SOUTH PECK ROAD
Manufacturer CityMONROVIA CA 91016
Manufacturer CountryUS
Manufacturer Postal91016
Manufacturer Phone6265744496
Manufacturer G1*
Manufacturer Street*
Manufacturer City*
Manufacturer Country*
Single Use3
Previous Use Code3
Event Type3
Type of Report3

Device Details

Brand NameTRANSBOND PLUS SELF ETCHING PRIMER
Generic NameORTHODONTIC ETCHANT/PRIMER
Product CodeDYH
Date Received2005-05-06
Model NumberNA
Catalog Number712-090
Lot NumberUNK
ID Number*
OperatorHEALTH PROFESSIONAL
Device AvailabilityN
Device Eval'ed by MfgrR
Implant FlagN
Date Removed*
Device Sequence No1
Device Event Key589627
Manufacturer3M UNITEK
Manufacturer Address2724 SOUTH PECK RD. MONROVIA CA 91016 US
Baseline Brand NameTRANSBOND PLUS SELF ETCHING PRIMER
Baseline Generic NameORTHODONTIC PRIMER
Baseline Model NoNA
Baseline Catalog No712-090
Baseline Device FamilyORTHODONTIC PRIMER
Baseline Shelf Life ContainedY
Baseline Shelf Life [Months]18
Baseline PMA FlagN
Baseline 510K PMNY
Premarket NotificationK001494
Baseline PreamendmentN
Baseline TransitionalN
510k ExemptN


Patients

Patient NumberTreatmentOutcomeDate
101. Required No Informationntervention 2005-05-06

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