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 health professional report with the FDA on 2020-03-24 for VISISTAT 35W 6/BOX 528235 manufactured by Teleflex Medical.

Event Text Entries

[184805763] (b)(4). The device history review for the product visistat 35w 6/box lot #73b1900440 investigation did not show issues related to the complaint. The device investigation is pending. Teleflex will continue to monitor and trend related events.
Patient Sequence No: 1, Text Type: N, H10


[184805764] It was reported that during an intervention the staples did not staple the skin.
Patient Sequence No: 1, Text Type: D, B5


MAUDE Entry Details

Report Number3003898360-2020-00282
MDR Report Key9873702
Report SourceHEALTH PROFESSIONAL
Date Received2020-03-24
Date of Report2020-03-02
Date of Event2020-03-02
Date Mfgr Received2020-03-02
Device Manufacturer Date2019-02-18
Date Added to Maude2020-03-24
Event Key0
Report Source CodeManufacturer report
Manufacturer LinkY
Number of Patients in Event0
Adverse Event Flag3
Product Problem Flag3
Reprocessed and Reused Flag3
Reporter OccupationRISK MANAGER
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 Received2020-03-24
Returned To Mfg2020-03-16
Catalog Number528235
Lot Number73B1900440
OperatorHEALTH PROFESSIONAL
Device AvailabilityR
Device Eval'ed by MfgrN
Device Sequence No1
Device Event Key0
ManufacturerTELEFLEX MEDICAL
Manufacturer AddressMORRISVILLE NC


Patients

Patient NumberTreatmentOutcomeDate
10 2020-03-24

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