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U.S. Department of Health and Human Services

MAUDE Adverse Event Report: BARD PERIPHERAL VASCULAR, INC. CROSSER RECANALIZATION CATHETER

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BARD PERIPHERAL VASCULAR, INC. CROSSER RECANALIZATION CATHETER Back to Search Results
Catalog Number CRU14SA
Device Problem Melted (1385)
Patient Problems No Consequences Or Impact To Patient (2199); No Known Impact Or Consequence To Patient (2692)
Event Type  Malfunction  
Event Description

It was reported that the recanalization catheter melted to the guide wire after approximately two minutes of activation in the tibial. The catheter and wire were removed together without incident. There was no reported pt injury.

 
Manufacturer Narrative

The lot number for the device has been provided. A review of the device history records is currently being performed. The device has been returned to the mfr for eval. The investigation is currently underway.

 
Manufacturer Narrative

The device history records were reviewed with special attention to the raw materials, subassemblies, manufacturing process and quality control testing. The lot met all release criteria. There was nothing found to indicate there was a manufacturing related cause for this event. The device was returned. The outer catheter was torn down its length starting at the rapid exchange junction and continuing proximal to the distal tip. A 45cm section of the guidewire lumen was returned separate from the catheter, with the distal portion twisted. The patency of the distal tip was tested with the returned guidewire and passed without issue. The guidewire and inner guidewire lumen were examined under a scope and no signs of melting were observed. Due to the poor sample condition, no further functional testing was performed. Per the reported details, the same user experienced 15 events over a short time period were the guidewire and catheters melted during use; therefore, the user's flowmate injector and generator were replaced and the user has not experienced the issue since. It is likely that the injector and/or generator contributed to the reported event; however, based upon the available information the definitive root cause is unk.

 
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Brand NameCROSSER RECANALIZATION CATHETER
Manufacturer (Section D)
BARD PERIPHERAL VASCULAR, INC.
tempe AZ
Manufacturer (Section G)
C.R.BARD, INC. (GFO)
289 bay road
queensbury NY 12804 2045
Manufacturer Contact
laura hintz
1625 west 3rd st.
tempe, AZ 85281
4808949515
MDR Report Key4905400
MDR Text Key6020074
Report Number2020394-2015-00999
Device Sequence Number1
Product Code DQY
Combination Product (Y/N)N
Reporter Country CodeUS
PMA/PMN NumberK072776
Number of Events Reported1
Summary Report (Y/N)N
Report Source Manufacturer
Source Type Company Representative,COMPANY REPRESENTATIVE
Reporter Occupation
Type of Report Initial,Followup
Report Date 05/01/2015
1 Device Was Involved in the Event
0 PatientS WERE Involved in the Event:
Date FDA Received07/06/2015
Is This An Adverse Event Report? No
Is This A Product Problem Report? Yes
Device Operator HEALTH PROFESSIONAL
Device EXPIRATION Date02/28/2017
Device Catalogue NumberCRU14SA
Device LOT NumberGFYL3007
Was Device Available For Evaluation? Yes
Date Returned to Manufacturer05/18/2015
Is The Reporter A Health Professional? Yes
Was the Report Sent to FDA?
Event Location No Information
Date Manufacturer Received06/05/2015
Was Device Evaluated By Manufacturer? Yes
Date Device Manufactured02/01/2015
Is The Device Single Use? Yes
Is this a Reprocessed and Reused Single-Use Device? No
Type of Device Usage Initial

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