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U.S. Department of Health and Human Services

MAUDE Adverse Event Report: MEDTRONIC IRELAND RELIANT BALLOON CATHETER, PERCUTANEOUS

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MEDTRONIC IRELAND RELIANT BALLOON CATHETER, PERCUTANEOUS Back to Search Results
Model Number AB46
Device Problem Adverse Event Without Identified Device or Use Problem (2993)
Patient Problems Cardiac Arrest (1762); Stroke/CVA (1770); Embolism (1829); Hemorrhage/Bleeding (1888); Myocardial Infarction (1969); Perforation (2001); Renal Failure (2041)
Event Type  Injury  
Manufacturer Narrative

If information is provided in the future, a supplemental report will be issued.

 
Event Description

Medtronic conducted a post market clinical follow-up (pmcf) survey to seek out potential new risks and assess performance of the reliant device. The exact size of the device is unknown. Survey results from an interventional cardiologist in practice 7 years, who has used the reliant device for expansion of vascular prostheses 250 times in total over the last 51 months and 30 times over the last 12 months and for temporary occlusion of large vessels 400 times in total over the last 51 months and 45 times over the last 12 months. During use of the reliant for expansion of vascular prostheses (assisting in the expansion of self-expanding stent grafts), the following complications were encountered; embolization with transient or permanent ischemia (small embolic formation in left pulmonary artery), vessel perforation or dissection (dehiscence ofa suture), stroke (patient with tia), cardiac events (ami in the system), haemorrhage(some bleeding with transfusions), renal complications (acute kidney failure (akf) on acute renal failure (arf) in 3 patients. The physician found the embolization with transient or permanent ischemia, cardiac events, haemorrhage somewhat or not at all concerning, vessel perforation or dissection, stroke, renal complications somewhat concerning. The stroke, cardiac events, haemorrhage and renal complications were reported to be not related to the device. Some of the embolization with transient or permanent ischemia, vessel perforation or dissection events were reported to be device related. During use of the reliant for temporary occlusion of large vessels, the following complications were encountered; cardiac events (systemic ami), hemorrhage (haemorrhage at the access site and transfusions). The physician found these events somewhat concerning or not all concerning (cardiac events). None of these events were reported to be related to the device. Of the above complications reported, some of these are listed as having been reported to medtronic previously. Due to limited information these are included in reporting. No further information has or will be provided.

 
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Brand NameRELIANT BALLOON
Type of DeviceCATHETER, PERCUTANEOUS
Manufacturer (Section D)
MEDTRONIC IRELAND
parkmore business park west
galway
Manufacturer (Section G)
MEDTRONIC IRELAND
parkmore business park west
galway
Manufacturer Contact
alison sweeney
parkmore business park west
galway 
091708096
MDR Report Key10028957
MDR Text Key197401993
Report Number9612164-2020-01798
Device Sequence Number1
Product Code DQY
Combination Product (Y/N)N
Reporter Country CodeIT
PMA/PMN NumberK050038
Number of Events Reported1
Summary Report (Y/N)N
Report Source Manufacturer
Source Type COMPANY REPRESENTATIVE,FOREIG
Reporter Occupation
Type of Report Initial,Followup
Report Date 06/08/2020
1 Device Was Involved in the Event
1 Patient Was Involved in the Event
Date FDA Received05/06/2020
Is This An Adverse Event Report? Yes
Is This A Product Problem Report? No
Device Operator HEALTH PROFESSIONAL
Device MODEL NumberAB46
Device Catalogue NumberAB46
Was Device Available For Evaluation? No
Is The Reporter A Health Professional? Yes
Was the Report Sent to FDA?
Event Location No Information
Date Manufacturer Received06/03/2020
Was Device Evaluated By Manufacturer? No Answer Provided
Is The Device Single Use? Yes
Is this a Reprocessed and Reused Single-Use Device? No
Type of Device Usage Initial

Patient TREATMENT DATA
Date Received: 05/06/2020 Patient Sequence Number: 1
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