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U.S. Department of Health and Human Services

MAUDE Adverse Event Report: VASCULAR SOLUTIONS, INC. GUARDIAN II; HEMOSTASIS VALVE

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VASCULAR SOLUTIONS, INC. GUARDIAN II; HEMOSTASIS VALVE Back to Search Results
Model Number FH101-T
Device Problem Device Operates Differently Than Expected (2913)
Patient Problem No Consequences Or Impact To Patient (2199)
Event Date 02/17/2016
Event Type  malfunction  
Manufacturer Narrative
Device not returned to manufacturer.
 
Event Description
A guardian ii hemostasis valve was used during a patient procedure.The valve did not close properly when pushed in.No patient impact was reported.
 
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Brand Name
GUARDIAN II
Type of Device
HEMOSTASIS VALVE
Manufacturer (Section D)
VASCULAR SOLUTIONS, INC.
6464 sycamore court north
maple grove MN 55369
Manufacturer (Section G)
VASCULAR SOLUTIONS, INC.
6464 sycamore court north
minneapolis MN 55369
Manufacturer Contact
renee michael
6464 sycamore court north
maple grove, MN 55369
7636564366
MDR Report Key5510754
MDR Text Key40686857
Report Number2134812-2016-00018
Device Sequence Number1
Product Code DTL
Combination Product (y/n)N
Reporter Country CodeIT
PMA/PMN Number
K122301
Number of Events Reported1
Summary Report (Y/N)N
Report Source Manufacturer
Source Type company representative,user f
Reporter Occupation Other
Remedial Action Recall
Type of Report Initial
Report Date 02/23/2016
1 Device was Involved in the Event
1 Patient was Involved in the Event
Date FDA Received03/18/2016
Is this an Adverse Event Report? No
Is this a Product Problem Report? Yes
Device Operator Physician
Device Expiration Date09/30/2018
Device Model NumberFH101-T
Device Lot Number42029
Was Device Available for Evaluation? No
Is the Reporter a Health Professional? No
Date Manufacturer Received02/23/2016
Was Device Evaluated by Manufacturer? Device Not Returned to Manufacturer
Date Device Manufactured09/30/2015
Is the Device Single Use? Yes
Type of Device Usage N
Removal/Correction Number2134812-03/16/2016-001R
Patient Sequence Number1
Patient Outcome(s) Other;
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