DELTON PIT & FISSURE SEALANT 27961

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a 00,01,05,07 report with the FDA on 2006-06-06 for DELTON PIT & FISSURE SEALANT 27961 manufactured by Dentsply Professional.

Event Text Entries

[20510442] A patient with no known allergies developed hives on the face and abdomen shortly after placement of delton sealant. The patient was referred to a specialist, though the treatment administered, if any, is unknown.
Patient Sequence No: 1, Text Type: D, B5


MAUDE Entry Details

Report Number2515379-2006-00275
MDR Report Key723156
Report Source00,01,05,07
Date Received2006-06-06
Date of Report2006-05-08
Date Mfgr Received2006-05-08
Date Added to Maude2006-06-08
Event Key0
Report Source CodeManufacturer report
Manufacturer LinkY
Number of Patients in Event0
Adverse Event Flag3
Product Problem Flag3
Reprocessed and Reused Flag3
Reporter OccupationDENTIST
Health Professional3
Initial Report to FDA3
Report to FDA3
Event Location0
Manufacturer ContactDR PATRICIA KIHN
Manufacturer Street221 W. PHILA. ST STE 60
Manufacturer CityYORK PA 17404
Manufacturer CountryUS
Manufacturer Postal17404
Manufacturer Phone7178457511
Manufacturer G1DENTSPLY CAULK
Manufacturer Street38 W. CLARKE AVE
Manufacturer CityMILFORD DE 19963
Manufacturer CountryUS
Manufacturer Postal Code19963
Single Use3
Previous Use Code3
Event Type3
Type of Report3

Device Details

Brand NameDELTON PIT & FISSURE SEALANT
Generic NameEBC
Product CodeEBC
Date Received2006-06-06
Model NumberNA
Catalog Number27961
Lot NumberUNK
ID NumberNA
OperatorHEALTH PROFESSIONAL
Device AvailabilityN
Device Eval'ed by MfgrR
Implant FlagN
Date Removed*
Device Sequence No1
Device Event Key712233
ManufacturerDENTSPLY PROFESSIONAL
Manufacturer Address* YORK PA * US
Baseline Brand NameDELTON PIT & FISSURE SEALANT LIGHT CURE
Baseline Generic NamePIT & FISSURE SEALANT AND CONDITIONER
Baseline Model NoNA
Baseline Catalog No27961
Baseline IDNA
Baseline Device FamilyCALIBRA
Baseline Shelf Life ContainedY
Baseline Shelf Life [Months]36
Baseline PMA FlagN
Baseline 510K PMNY
Premarket NotificationK831380
Baseline PreamendmentN
Baseline TransitionalN
510k ExemptN


Patients

Patient NumberTreatmentOutcomeDate
101. Other 2006-06-06

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