ENTACT SEPTAL STAPLER, 1-PACK 601-00100S

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed with the FDA on 2018-07-31 for ENTACT SEPTAL STAPLER, 1-PACK 601-00100S manufactured by Arthrocare Corporation.

Event Text Entries

[115774018]
Patient Sequence No: 1, Text Type: N, H10


[115774019] It was reported that the first stapler failed to dispense any sutures, back up device was used and sutures did not stay in the septum. A delay greater than 30 minutes was reported. No patient injuries were reported. Local anesthesia was used.
Patient Sequence No: 1, Text Type: D, B5


MAUDE Entry Details

Report Number3006524618-2018-00394
MDR Report Key7736260
Date Received2018-07-31
Date of Report2018-08-02
Date of Event2018-05-25
Date Mfgr Received2018-08-01
Date Added to Maude2018-07-31
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 ContactJIM GONZALES
Manufacturer Street7000 WEST WILLIAM CANNON DRIVE
Manufacturer CityAUSTIN TX 78735
Manufacturer CountryUS
Manufacturer Postal78735
Manufacturer Phone5123585706
Manufacturer G1ARTHROCARE CORPORATION
Manufacturer Street7000 WEST WILLIAM CANNON DRIVE
Manufacturer CityAUSTIN TX 78735
Manufacturer CountryUS
Manufacturer Postal Code78735
Single Use3
Previous Use Code3
Event Type3
Type of Report0

Device Details

Brand NameENTACT SEPTAL STAPLER, 1-PACK
Generic NameSEPTAL STAPLER/ABSORBABLE STAPLES
Product CodeOLL
Date Received2018-07-31
Catalog Number601-00100S
OperatorHEALTH PROFESSIONAL
Device AvailabilityN
Device AgeDA
Device Eval'ed by MfgrN
Device Sequence No1
Device Event Key0
ManufacturerARTHROCARE CORPORATION
Manufacturer Address7000 WEST WILLIAM CANNON DRIVE AUSTIN TX 78735 US 78735


Patients

Patient NumberTreatmentOutcomeDate
10 2018-07-31

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