DISP FIRSTPASS STR PASSR SELF 22-4038

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed with the FDA on 2019-10-14 for DISP FIRSTPASS STR PASSR SELF 22-4038 manufactured by Arthrocare Corp..

Event Text Entries

[167662467] It was reported that during the procedure the surgeon was able to fire the needle using the triggers, but the needle did not return to the initial position. No patient injuries or delay reported. Back-up device was not available.
Patient Sequence No: 1, Text Type: D, B5


MAUDE Entry Details

Report Number3006524618-2019-00507
MDR Report Key9189226
Date Received2019-10-14
Date of Report2019-10-14
Date of Event2019-09-30
Date Mfgr Received2019-10-01
Device Manufacturer Date2018-11-12
Date Added to Maude2019-10-14
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 Report0

Device Details

Brand NameDISP FIRSTPASS STR PASSR SELF
Generic NamePASSER
Product CodeHWQ
Date Received2019-10-14
Catalog Number22-4038
Lot Number2023580
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 2019-10-14

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