BLUNTPORT PLUS 179775P

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a foreign,user facility report with the FDA on 2017-04-27 for BLUNTPORT PLUS 179775P manufactured by Davis & Geck Caribe Ltd.

Event Text Entries

[73821076]
Patient Sequence No: 1, Text Type: N, H10


[73821077] According to the reporter, prior to use, the nurse found rubber packing in the grip disengaged. The device was not used on the patient. The procedure was completed with another device.
Patient Sequence No: 1, Text Type: D, B5


MAUDE Entry Details

Report Number9612501-2017-05395
MDR Report Key6525605
Report SourceFOREIGN,USER FACILITY
Date Received2017-04-27
Date of Report2017-03-28
Date of Event2017-03-28
Date Mfgr Received2017-03-28
Device Manufacturer Date2016-08-23
Date Added to Maude2017-04-27
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 ContactSHARON MURPHY
Manufacturer Street60 MIDDLETOWN AVE
Manufacturer CityNORTH HAVEN CT 06473
Manufacturer CountryUS
Manufacturer Postal06473
Manufacturer Phone2034925267
Manufacturer G1DAVIS & GECK CARIBE LTD
Manufacturer StreetZONA FRANCA DE SAN ISIDRO
Manufacturer CitySANTO DOMINGO 0101
Manufacturer CountryDO
Manufacturer Postal Code0101
Single Use3
Previous Use Code3
Event Type3
Type of Report3

Device Details

Brand NameBLUNTPORT PLUS
Generic NameGOUGE, SURGICAL, GENERAL & PLASTIC SURGERY
Product CodeGDH
Date Received2017-04-27
Model Number179775P
Catalog Number179775P
Lot NumberJ6H2004X
OperatorHEALTH PROFESSIONAL
Device AvailabilityN
Device Eval'ed by Mfgr*
Device Sequence No1
Device Event Key0
ManufacturerDAVIS & GECK CARIBE LTD
Manufacturer AddressZONA FRANCA DE SAN ISIDRO SANTO DOMINGO 0101 DO 0101


Patients

Patient NumberTreatmentOutcomeDate
10 2017-04-27

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