AMBIENT SUPER MULTIVAC 50 IFS ASHA4830-01

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a company representative,user f report with the FDA on 2020-03-29 for AMBIENT SUPER MULTIVAC 50 IFS ASHA4830-01 manufactured by Arthrocare Corp..

Event Text Entries

[185501455] It was reported that during knee arthroscopy part of the metal screen on the tip of the wand broke off inside the joint. A shaver was used to retrieved the small fragment. No patient injuries or significant delay reported. Back-up device was available to complete the surgery. All available information has been disclosed. If additional information should become available, a supplemental report will be submitted accordingly.
Patient Sequence No: 1, Text Type: D, B5


MAUDE Entry Details

Report Number3006524618-2020-00137
MDR Report Key9896234
Report SourceCOMPANY REPRESENTATIVE,USER F
Date Received2020-03-29
Date of Report2020-03-29
Date of Event2020-03-06
Date Mfgr Received2020-03-06
Device Manufacturer Date2018-02-23
Date Added to Maude2020-03-29
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 ContactHOLLY TOPPING
Manufacturer Street7000 WEST WILLIAM CANNON DRIVE
Manufacturer CityAUSTIN TX 78735
Manufacturer CountryUS
Manufacturer Postal78735
Manufacturer Phone5123913905
Manufacturer G1ARTHROCARE CORP.
Manufacturer Street7000 W. WILLIAM CANNON
Manufacturer CityAUSTIN TX 78735
Manufacturer CountryUS
Manufacturer Postal Code78735
Single Use3
Previous Use Code3
Event Type3
Type of Report3

Device Details

Brand NameAMBIENT SUPER MULTIVAC 50 IFS
Generic NameELECTROSURGICAL, CUTTING & COAGULATION & ACCESSORIES
Product CodeGEI
Date Received2020-03-29
Model NumberASHA4830-01
Catalog NumberASHA4830-01
Lot Number2011312
OperatorHEALTH PROFESSIONAL
Device AvailabilityN
Device Eval'ed by Mfgr*
Device Sequence No1
Device Event Key0
ManufacturerARTHROCARE CORP.
Manufacturer Address7000 W. WILLIAM CANNON AUSTIN TX 78735 US 78735


Patients

Patient NumberTreatmentOutcomeDate
10 2020-03-29

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