RANEY SCALP CLIP DISPOSE

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a company representative,foreig report with the FDA on 2015-12-03 for RANEY SCALP CLIP DISPOSE manufactured by .

Event Text Entries

[32665104] Gtin: unknown. Upon completion of the investigation, a follow up report will be filed.
Patient Sequence No: 1, Text Type: N, H10


[32665105] A foreign matter (metal fragment) was found in the package of the device during pre-use inspection. There were no adverse consequences associated with this event.
Patient Sequence No: 1, Text Type: D, B5


MAUDE Entry Details

Report Number1226348-2015-10728
MDR Report Key5265432
Report SourceCOMPANY REPRESENTATIVE,FOREIG
Date Received2015-12-03
Date of Event2015-11-11
Date Mfgr Received2015-11-12
Date Added to Maude2015-12-03
Event Key0
Report Source CodeManufacturer report
Manufacturer LinkY
Number of Patients in Event0
Adverse Event Flag3
Product Problem Flag3
Reprocessed and Reused Flag3
Reporter OccupationMEDICAL EQUIPMENT COMPANY TECHNICIAN/REPRESENTATIVE
Health Professional3
Initial Report to FDA3
Report to FDA3
Event Location3
Manufacturer ContactMR JAMES KENNEY
Manufacturer Street325 PARAMOUNT DRIVE
Manufacturer CityRAYNHAM MA 02767
Manufacturer CountryUS
Manufacturer Postal02767
Manufacturer Phone5088282726
Single Use3
Previous Use Code3
Event Type3
Type of Report3

Device Details

Brand NameRANEY SCALP CLIP DISPOSE
Generic NameCLIPS, SCALP
Product CodeHBO
Date Received2015-12-03
Returned To Mfg2015-11-18
Lot NumberBH606
OperatorHEALTH PROFESSIONAL
Device AvailabilityR
Device Eval'ed by MfgrN
Device Sequence No1
Device Event Key0
Manufacturer AddressUS


Patients

Patient NumberTreatmentOutcomeDate
10 2015-12-03

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