VASCU-GUARD VG0108N

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a company representative report with the FDA on 2020-02-21 for VASCU-GUARD VG0108N manufactured by Baxter Healthcare Corporation.

Event Text Entries

[180516267] Should additional relevant information become available, a supplemental report will be submitted.
Patient Sequence No: 1, Text Type: N, H10


[180516268] It was reported that hair was observed on a vascu-guard patch. This issue was identified during setup and prior to patient use. There was no patient involvement. No additional information is available.
Patient Sequence No: 1, Text Type: D, B5


MAUDE Entry Details

Report Number1416980-2020-00893
MDR Report Key9742341
Report SourceCOMPANY REPRESENTATIVE
Date Received2020-02-21
Date of Report2020-03-25
Date of Event2020-01-29
Date Mfgr Received2020-03-10
Date Added to Maude2020-02-21
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 Street25212 W. ILLINOIS ROUTE 120
Manufacturer CityROUND LAKE IL 60073
Manufacturer CountryUS
Manufacturer Postal60073
Manufacturer Phone2242702068
Manufacturer G1SYNOVIS SURGICAL INNOVATIONS
Manufacturer Street2575 UNIVERSITY AVE. W
Manufacturer CitySAINT PAUL MN 55114
Manufacturer CountryUS
Manufacturer Postal Code55114
Single Use3
Previous Use Code3
Event Type3
Type of Report3

Device Details

Brand NameVASCU-GUARD
Generic NamePATCH, PLEDGET AND INTRACARDIAC, PETP, PTFE, POLYPROPYLENE
Product CodeDXZ
Date Received2020-02-21
Model NumberNA
Catalog NumberVG0108N
Lot NumberSP19L06-1415539
Device AvailabilityN
Device AgeDA
Device Eval'ed by MfgrR
Device Sequence No1
Device Event Key0
ManufacturerBAXTER HEALTHCARE CORPORATION
Manufacturer AddressDEERFIELD IL


Patients

Patient NumberTreatmentOutcomeDate
10 2020-02-21

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