DISP BIOPSY PUNCHES 3MM 33-32

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed with the FDA on 2015-11-25 for DISP BIOPSY PUNCHES 3MM 33-32 manufactured by Integra York, Pa Inc..

Event Text Entries

[32300031] To date the device involved in the reported incident has not been received for evaluation. An investigation has been initiated based on the reported information.
Patient Sequence No: 1, Text Type: N, H10


[32300032] Customer initially reports that the packaging on 1 pc was punctured when they removed it from the box.
Patient Sequence No: 1, Text Type: D, B5


MAUDE Entry Details

Report Number1722447-2015-00013
MDR Report Key5250851
Date Received2015-11-25
Date of Report2015-11-10
Date Mfgr Received2015-11-10
Device Manufacturer Date2015-06-01
Date Added to Maude2015-11-25
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 Location3
Manufacturer ContactUSER SANDRA LEE
Manufacturer Street311 ENTERPRISE DRIVE
Manufacturer CityPLAINSBORO NJ 08536
Manufacturer CountryUS
Manufacturer Postal08536
Manufacturer Phone6099362393
Manufacturer G1INTEGRA YORK, PA INC.
Manufacturer Street589 DAVIES DRIVE
Manufacturer CityYORK PA 17402
Manufacturer CountryUS
Manufacturer Postal Code17402
Single Use3
Previous Use Code3
Event Type3
Type of Report0

Device Details

Brand NameDISP BIOPSY PUNCHES 3MM
Generic NameM3 - DERMAL
Product CodeJYG
Date Received2015-11-25
Returned To Mfg2015-11-17
Catalog Number33-32
Lot NumberUNKNOWN
OperatorHEALTH PROFESSIONAL
Device AvailabilityR
Device AgeDA
Device Eval'ed by MfgrY
Device Sequence No1
Device Event Key0
ManufacturerINTEGRA YORK, PA INC.
Manufacturer Address589 DAVIES DRIVE 589 DAVIES DRIVE YORK PA 17402 US 17402


Patients

Patient NumberTreatmentOutcomeDate
10 2015-11-25

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