VISISTAT 35W 6/BOX 528235

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a foreign,health professional report with the FDA on 2020-03-06 for VISISTAT 35W 6/BOX 528235 manufactured by Teleflex Medical.

Event Text Entries

[182431506] (b)(4). The device has not been returned for investigation. Teleflex will continue to monitor and trend related events.
Patient Sequence No: 1, Text Type: N, H10


[182431507] It was reported that the staples will not close properly.
Patient Sequence No: 1, Text Type: D, B5


MAUDE Entry Details

Report Number3003898360-2020-00269
MDR Report Key9800952
Report SourceFOREIGN,HEALTH PROFESSIONAL
Date Received2020-03-06
Date of Report2020-02-17
Date of Event2020-02-13
Date Mfgr Received2020-02-17
Date Added to Maude2020-03-06
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 ContactEFFIE JEFFERSON
Manufacturer Street3015 CARRINGTON MILL BLVD
Manufacturer CityMORRISVILLE 27560
Manufacturer CountryUS
Manufacturer Postal27560
Manufacturer Phone9194332672
Manufacturer G1TELEFLEX MEDICAL
Manufacturer StreetRANCHO EL DESCANSO
Manufacturer CityTECATE 21478
Manufacturer CountryMX
Manufacturer Postal Code21478
Single Use3
Previous Use Code3
Event Type3
Type of Report3

Device Details

Brand NameVISISTAT 35W 6/BOX
Generic NameSTAPLE, REMOVABLE (SKIN)
Product CodeGDT
Date Received2020-03-06
Catalog Number528235
Lot Number73C190074
OperatorHEALTH PROFESSIONAL
Device AvailabilityY
Device Eval'ed by MfgrR
Device Sequence No1
Device Event Key0
ManufacturerTELEFLEX MEDICAL
Manufacturer AddressMORRISVILLE NC


Patients

Patient NumberTreatmentOutcomeDate
10 2020-03-06

© 2024 FDA.report
This site is not affiliated with or endorsed by the FDA.