FDA Device recall Z-2317-2015

Beacon Tip Torcon NB Advantage Catheter

FDA Device
Class I
terminated
Published 2015-08-12

On 2015-08-12 the FDA classified a Class I recall of Beacon Tip Torcon NB Advantage Catheter by Cook, citing reports of catheter tip splits and or separation. Loss of device function, medical intervention to retrieve separated segment, or complications resulting from separated tip occlud….

Read the official FDA Device notice

Agency	FDA Device
Recall number	Z-2317-2015
Classification	Class I
Status	terminated
Initiated	2015-07-02
Published	2015-08-12
Last updated	2026-09-13 11:53 UTC
Company	Cook
Distribution	US

Product

Beacon Tip Torcon NB Advantage Catheter. Angiographic catheter. For use in angiographic procedures as a conduit for the delivery of contrast media and can help physicians diagnose occlusion or stenosis. The catheters are designed for percutaneous introduction into the vascular system over an appropriately sized wire guide.

Reason

Reports of catheter tip splits and or separation. Loss of device function, medical intervention to retrieve separated segment, or complications resulting from separated tip occluding blood flow to end organs may result.

Identifiers

code_info	All Lots of following Product numbers: HNBR4.0-35-100-P-NS-0, HNBR4.0-35-100-P-NS-C1, HNBR4.0-35-100-P-NS-C2, HNBR… All Lots of following Product numbers: HNBR4.0-35-100-P-NS-0, HNBR4.0-35-100-P-NS-C1, HNBR4.0-35-100-P-NS-C2, HNBR4.0-35-100-P-NS-CANADA-041480, HNBR4.0-35-100-P-NS-DAV, HNBR4.0-35-100-P-NS-H1, HNBR4.0-35-100-P-NS-JB1, HNBR4.0-35-100-P-NS-JB2, HNBR4.0-35-100-P-NS-JB3, HNBR4.0-35-100-P-NS-JIM, HNBR4.0-35-100-P-NS-KMP, HNBR4.0-35-100-P-NS-MPA, HNBR4.0-35-100-P-NS-O1, HNBR4.0-35-100-P-NS-SIM1, HNBR4.0-35-100-P-NS-SIM2, HNBR4.0-35-100-P-NS-SIM3, HNBR4.0-35-100-P-NS-VERT, HNBR4.0-35-100-P-NS-VTK, HNBR4.0-35-100-P-NS-WNBG, HNBR4.0-35-125-P-NS-0, HNBR4.0-35-125-P-NS-DAV, HNBR4.0-35-125-P-NS-H1, HNBR4.0-35-125-P-NS-JB1, HNBR4.0-35-125-P-NS-JB2, HNBR4.0-35-125-P-NS-MPA, HNBR4.0-35-125-P-NS-SIM2, HNBR4.0-35-125-P-NS-VERT, HNBR4.0-35-125-P-NS-VTK, HNBR4.0-35-125-P-NS-WNBG, HNBR4.0-35-40-P-NS-KMP, HNBR4.0-35-65-P-NS-0, HNBR4.0-35-65-P-NS-C1, HNBR4.0-35-65-P-NS-C2, HNBR4.0-35-65-P-NS-C3, HNBR4.0-35-65-P-NS-DAV, HNBR4.0-35-65-P-NS-H1, HNBR

code_info

All Lots of following Product numbers: HNBR4.0-35-100-P-NS-0, HNBR4.0-35-100-P-NS-C1, HNBR4.0-35-100-P-NS-C2, HNBR…

All Lots of following Product numbers: HNBR4.0-35-100-P-NS-0, HNBR4.0-35-100-P-NS-C1, HNBR4.0-35-100-P-NS-C2, HNBR4.0-35-100-P-NS-CANADA-041480, HNBR4.0-35-100-P-NS-DAV, HNBR4.0-35-100-P-NS-H1, HNBR4.0-35-100-P-NS-JB1, HNBR4.0-35-100-P-NS-JB2, HNBR4.0-35-100-P-NS-JB3, HNBR4.0-35-100-P-NS-JIM, HNBR4.0-35-100-P-NS-KMP, HNBR4.0-35-100-P-NS-MPA, HNBR4.0-35-100-P-NS-O1, HNBR4.0-35-100-P-NS-SIM1, HNBR4.0-35-100-P-NS-SIM2, HNBR4.0-35-100-P-NS-SIM3, HNBR4.0-35-100-P-NS-VERT, HNBR4.0-35-100-P-NS-VTK, HNBR4.0-35-100-P-NS-WNBG, HNBR4.0-35-125-P-NS-0, HNBR4.0-35-125-P-NS-DAV, HNBR4.0-35-125-P-NS-H1, HNBR4.0-35-125-P-NS-JB1, HNBR4.0-35-125-P-NS-JB2, HNBR4.0-35-125-P-NS-MPA, HNBR4.0-35-125-P-NS-SIM2, HNBR4.0-35-125-P-NS-VERT, HNBR4.0-35-125-P-NS-VTK, HNBR4.0-35-125-P-NS-WNBG, HNBR4.0-35-40-P-NS-KMP, HNBR4.0-35-65-P-NS-0, HNBR4.0-35-65-P-NS-C1, HNBR4.0-35-65-P-NS-C2, HNBR4.0-35-65-P-NS-C3, HNBR4.0-35-65-P-NS-DAV, HNBR4.0-35-65-P-NS-H1, HNBR

Status history

No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:53 UTC. Current status: terminated.

Source

Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2317-2015%22

RecallRadar indexes public recall notices from the FDA, USDA FSIS, and CPSC. The official agency notice is the authoritative source. Always confirm details at the linked source before acting.