Z-2317-2015 Class I Terminated
Recalled by Cook Inc.
— Bloomington, IN
FDA device recall Z-2317-2015 was initiated by Cook Inc. on Jul 2, 2015 and is designated Class I. Reason for recall: 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… The recall status is terminated (terminated Sep 2, 2017). Affected quantity: 451550.
Recall Details
- Product Type
- Devices
- Report Date
- Aug 12, 2015
- Initiation Date
- Jul 2, 2015
- Termination Date
- Sep 2, 2017
- Voluntary/Mandated
- Voluntary: Firm initiated
- Product Quantity
- 451550
Product Description
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 for Recall
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.
Distribution Pattern
Worldwide Distribution - US (nationwide including Puerto Rico and US Virgin Islands), Algeria, Antigua, Armenia, Austria, Australia, Bahamas, Belgium, Bangladesh, Bulgaria, Bahrain, Brazil, Brunei Darussalam, Canada, Canary Islands, Chile, China, Colombia, Costa Rica, Cyprus, Czech Republic, Denmark, Dominican Republic, Egypt, El Salvador, Finland, France, French Polynesia, Georgia, Germany, Ghana, Great Britain, Greece Guadeloupe, Hong Kong, Hungary, Iceland, India, Indonesia, Iraq, Ireland, Israel, Italy, Japan, Jersey, Jordan, Kuwait, Kazakhstan, Republic of Korea, Kuwait, Lebanon, Lithuania, Luxemburg, Latvia, Libya, Macau, Malaysia, Malta, Martinique, Mexico, Mongolia, Morocco, Netherlands, Netherlands Antilles, New Caledonia, New Zealand, Nicaragua, Norway, Oman, Pakistan, Panama, Paraguay, Peru, Philippines, Poland, Portugal, Qatar, Reunion, Romania, Russian Federation, Saudi Arabia, Serbia, Singapore, Slovakia, Slovenia, South Africa, Sri Lanka, Sweden, Switzerland, Spain, Taiwan, Thailand, Turkey, Ukraine, United Arab Emirates, United Kingdom, Uruguay, Venezuela, and Vietnam.
Code Information
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, HNBR4.0-35-65-P-NS-JB1, HNBR4.0-35-65-P-NS-KMP, HNBR4.0-35-65-P-NS-MPA, HNBR4.0-35-65-P-NS-RC1, HNBR4.0-35-65-P-NS-RC2, HNBR4.0-35-65-P-NS-RDC, HNBR4.0-35-65-P-NS-RIM, HNBR4.0-35-65-P-NS-SIM1, HNBR4.0-35-65-P-NS-SIM2, HNBR4.0-35-80-P-NS-C1, HNBR4.0-35-80-P-NS-C2, HNBR4.0-35-80-P-NS-JL2, HNBR4.0-35-80-P-NS-JL2.5, HNBR4.0-35-80-P-NS-JL3, HNBR4.0-35-80-P-NS-JR1, HNBR4.0-35-80-P-NS-JR2, HNBR4.0-35-80-P-NS-JR3.5, HNBR4.0-35-80-P-NS-RH, HNBR4.0-35-80-P-NS-RLG, HNBR4.0-35-80-P-NS-VS, HNBR4.0-35-80-P-NS-VS1, HNBR4.0-35-80-P-NS-VS2, HNBR4.0-35-80-P-NS-VS3, HNBR4.0-NT-100-P-NS-H1, HNBR4.0-NT-80-P-NS-RC1, HNBR4.0-NT-80-P-NS-RIM, HNBR4.0-NT-80-P-NS-RLG, HNBR4.1-35-100-P-NS-0, HNBR4.1-35-100-P-NS-C1, HNBR4.1-35-100-P-NS-C2, HNBR4.1-35-100-P-NS-DAV, HNBR4.1-35-100-P-NS-H1, HNBR4.1-35-100-P-NS-JB1, HNBR4.1-35-100-P-NS-JB2, HNBR4.1-35-100-P-NS-JB3, HNBR4.1-35-100-P-NS-KMP, HNBR4.1-35-100-P-NS-MPA, HNBR4.1-35-100-P-NS-O1, HNBR4.1-35-100-P-NS-SIM1, HNBR4.1-35-100-P-NS-SIM2, HNBR4.1-35-100-P-NS-SIM3, HNBR4.1-35-100-P-NS-VERT, HNBR4.1-35-100-P-NS-WNBG, HNBR4.1-35-110-P-NS-JB1, HNBR4.1-35-110-P-NS-JB2, HNBR4.1-35-110-P-NS-WNBG, HNBR4.1-35-120-P-NS-JB2, HNBR4.1-35-130-P-NS-DAV-T, HNBR4.1-35-40-P-NS-KMP, HNBR4.1-35-65-P-NS-C1, HNBR4.1-35-65-P-NS-C2, HNBR4.1-35-65-P-NS-DAV, HNBR4.1-35-65-P-NS-H1, HNBR4.1-35-65-P-NS-JB1, HNBR4.1-35-65-P-NS-KMP, HNBR4.1-35-65-P-NS-LEV1, HNBR4.1-35-65-P-NS-MPA, HNBR4.1-35-65-P-NS-RC1, HNBR4.1-35-65-P-NS-RC2, HNBR4.1-35-65-P-NS-RDC, HNBR4.1-35-65-P-NS-RIM, HNBR4.1-35-65-P-NS-SHK1.0, HNBR4.1-35-65-P-NS-SIM1, HNBR4.1-35-75-P-NS-CHG-D, HNBR4.1-35-80-P-NS-C1, HNBR4.1-35-80-P-NS-C2, HNBR4.1-35-80-P-NS-JL2, HNBR4.1-35-80-P-NS-JL2.5, HNBR4.1-35-80-P-NS-JL3, HNBR4.1-35-80-P-NS-JR1, HNBR4.1-35-80-P-NS-JR2, HNBR4.1-35-80-P-NS-JR3.5, HNBR4.1-35-80-P-NS-RC1, HNBR4.1-35-80-P-NS-RH, HNBR4.1-35-80-P-NS-RLG, HNBR4.1-35-80-P-NS-VS, HNBR4.1-35-80-P-NS-VS2, HNBR4.1-NT-100-P-NS-H1, HNBR4.1-NT-80-P-NS-C1, HNBR4.1-NT-80-P-NS-RC1, HNBR4.1-NT-80-P-NS-RH, HNBR4.1-NT-80-P-NS-RIM, HNBR4.1-NT-80-P-NS-RLG, HNBR5.0-35-65-P-NS-RUC, HNBR5.0-35-90-P-NS-RUC
Source
- Dataset
- openFDA device recall enforcement reports
- FDA record
- This recall in openFDA (JSON)
- Enforcement Report
- Search FDA's Enforcement Report for Z-2317-2015
- openFDA file date
- Oct 23, 2026
- Loaded by RegDataLab
- Oct 26, 2026
These dates say when openFDA published the data file and when RegDataLab last loaded it.