TOOTH CONDITIONER GEL 646125

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 2001-05-14 for TOOTH CONDITIONER GEL 646125 manufactured by L.d. Caulk.

Event Text Entries

[206915] The dentist was expressing the material when the tip came off of the syringe and the material went into the dental assistant's eye. The assistant went to the emergency room and was treated for a corneal burn.
Patient Sequence No: 1, Text Type: D, B5


MAUDE Entry Details

Report Number2515379-2001-00006
MDR Report Key333074
Report Source05
Date Received2001-05-14
Date of Report2001-04-26
Date of Event2001-03-26
Date Added to Maude2001-05-18
Event Key0
Report Source CodeManufacturer report
Manufacturer LinkY
Number of Patients in Event0
Adverse Event Flag3
Product Problem Flag3
Reprocessed and Reused Flag0
Reporter OccupationDENTIST
Health Professional3
Initial Report to FDA3
Report to FDA3
Event Location0
Manufacturer ContactWILLIAM FREY, JR.
Manufacturer Street570 W. COLLEGE AVENUE P.O. BOX 872
Manufacturer CityYORK PA 174050872
Manufacturer CountryUS
Manufacturer Postal174050872
Manufacturer Phone7178457511
Manufacturer G1*
Manufacturer Street*
Manufacturer City*
Manufacturer Country*
Single Use3
Previous Use Code3
Event Type3
Type of Report3

Device Details

Brand NameTOOTH CONDITIONER GEL
Generic NameDENTAL RESTORATIVE MATERIAL
Product CodeEBC
Date Received2001-05-14
Model NumberNA
Catalog Number646125
Lot Number000906
ID NumberNA
OperatorHEALTH PROFESSIONAL
Device AvailabilityN
Device Eval'ed by MfgrR
Implant FlagN
Date RemovedA
Device Sequence No1
Device Event Key322448
ManufacturerL.D. CAULK
Manufacturer Address38 W. CLARKE AVENUE PO BOX 359 MILFORD DE 199630359 US
Baseline Brand NameCAULK TOOTH CONDITION GEL 34%
Baseline Generic NamePIT AND FISSURE SEALANT AND CONDITIONER
Baseline Model NoNA
Baseline Catalog No646125
Baseline IDNA
Baseline Device FamilyNA
Baseline Shelf Life Contained*
Baseline Shelf Life [Months]*
Baseline PMA FlagN
Baseline 510K PMNY
Premarket NotificationK942031
Baseline PreamendmentN
Baseline TransitionalN
510k ExemptN


Patients

Patient NumberTreatmentOutcomeDate
101. Required No Informationntervention 2001-05-14

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