COLLATAPE

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a 05,06,08 report with the FDA on 2013-05-20 for COLLATAPE manufactured by Integra Lifesciences Corp..

Event Text Entries

[21983605] It was reported "the doctor states several of his patients had infections and the implants failed due to the affected product. " add'l info was requested by integra.
Patient Sequence No: 1, Text Type: D, B5


[22340902] The device involved in the reported incident is not expected to be received for eval. An investigation has been initiated based upon the reported info.
Patient Sequence No: 1, Text Type: N, H10


MAUDE Entry Details

Report Number1121308-2013-00013
MDR Report Key3126766
Report Source05,06,08
Date Received2013-05-20
Date of Report2013-05-20
Date Mfgr Received2013-05-07
Date Added to Maude2013-05-24
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 ContactCAREN FINKELSTEIN
Manufacturer Street315 ENTERPRISE DRIVE
Manufacturer CityPLAINSBORO NJ 08536
Manufacturer CountryUS
Manufacturer Postal08536
Manufacturer Phone6099362341
Manufacturer G1INTEGRA LIFESCIENCES CORP.
Manufacturer Street315 ENTERPRISE DRIVE
Manufacturer CityPLAINSBORO NJ 08536
Manufacturer CountryUS
Manufacturer Postal Code08536
Single Use3
Previous Use Code3
Event Type3
Type of Report3

Device Details

Brand NameCOLLATAPE
Generic NameDENTAL PRODUCTS
Product CodeLPG
Date Received2013-05-20
Lot Number1125686
OperatorHEALTH PROFESSIONAL
Device AvailabilityN
Device AgeDA
Device Eval'ed by MfgrR
Device Sequence No1
Device Event Key0
ManufacturerINTEGRA LIFESCIENCES CORP.
Manufacturer Address105 MORGAN LANE PLAINSBORO NJ 08536 US 08536


Patients

Patient NumberTreatmentOutcomeDate
101. Other 2013-05-20

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