D-STAT FLOWABLE HEMOSTAT 4000 *

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a 04,05,06,07 report with the FDA on 2007-04-27 for D-STAT FLOWABLE HEMOSTAT 4000 * manufactured by Vascular Solutions, Inc..

Event Text Entries

[629298] A liver biopsy was performed and d-stat flowable was deployed into the tissue tract. After deployment, the pt immediately turned bright red, became hypertensive and was short of breath. For treatment, the pt was given intravenous antihistamine and within 30 mins she had normal vital signs. The pt was later discharged with no further complications. The physician later stated that he may have inadvertently injected the flowable into the portal vein, which caused an anaphylactive reaction in the pt. Please note that use of the d-stat flowable prod in this manner represented an off-label use of the product.
Patient Sequence No: 1, Text Type: D, B5


[7927560] The device was used for an unapproved indication.
Patient Sequence No: 1, Text Type: N, H10


MAUDE Entry Details

Report Number2134812-2007-00004
MDR Report Key842966
Report Source04,05,06,07
Date Received2007-04-27
Date of Report2007-04-27
Date of Event2007-04-04
Date Mfgr Received2007-04-18
Date Added to Maude2007-05-02
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 Location0
Manufacturer ContactJULIE TAPPER
Manufacturer Street6464 SYCAMORE CT.
Manufacturer CityMINNEAPOLIS MN 55369
Manufacturer CountryUS
Manufacturer Postal55369
Manufacturer Phone7636564228
Manufacturer G1*
Manufacturer Street*
Manufacturer City*
Manufacturer Country*
Single Use3
Previous Use Code3
Event Type3
Type of Report3

Device Details

Brand NameD-STAT FLOWABLE HEMOSTAT
Generic NameTOPICAL HEMOSTAT
Product CodeMHW
Date Received2007-04-27
Model Number4000
Catalog Number*
Lot NumberUNK.
ID Number*
OperatorHEALTH PROFESSIONAL
Device AvailabilityN
Device Eval'ed by MfgrR
Implant FlagN
Date Removed*
Device Sequence No1
Device Event Key830102
ManufacturerVASCULAR SOLUTIONS, INC.
Manufacturer Address* MINNEAPOLIS MN 55369 US


Patients

Patient NumberTreatmentOutcomeDate
101. Other 2007-04-27

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