FDA Device recall Z-1390-2017
Flexor Radial Access Set, Individual product is packaged in a Tyvek-film sterilizable outer pouch
- FDA Device
- Class II
- terminated
- Published 2017-03-08
On 2017-03-08 the FDA classified a Class II recall of Flexor Radial Access Set, Individual product is packaged in a Tyvek-film sterilizable outer pouch by Cook, citing devices using a specific hemostatic valve design, referred to as a blue valve or polyisoprene valve, have an increase in reports of blood loss associated with the devices which co….
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-1390-2017 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2017-02-01 |
| Published | 2017-03-08 |
| Last updated | 2026-09-13 11:54 UTC |
| Company | Cook |
| Distribution | AL, AR, AZ, CA, CO, CT, DE, FL, GA, HI, IA, ID, IL, IN, KS, KY, LA, MA, MD, ME, MI, MN, MO, MS, MT, NC, NE, NH, NJ, NM, NV, NY, OH, OK, OR, PA, RI, SC, SD, TN, TX, UT, VA, WA, WI, WV |
Product
Flexor Radial Access Set, Individual product is packaged in a Tyvek-film sterilizable outer pouch. The Flexor¿ Radial Hydrophilic Introducer Access Set is intended to introduce diagnostic and interventional devices In radial artery access procedures
Reason
Devices using a specific hemostatic valve design, referred to as a blue valve or polyisoprene valve, have an increase in reports of blood loss associated with the devices which could result in delay in procedure and blood loss from patients.
Identifiers
| code_info | Catalog Identifier: KCFN-4.0(5.0,6.0,7.0)- / -RA-(S)-HC Codes consist of Lot #, RPN #, Manufacture Date and Expirati…Catalog Identifier: KCFN-4.0(5.0,6.0,7.0)- / -RA-(S)-HC Codes consist of Lot #, RPN #, Manufacture Date and Expiration Date: 4427564X KCFN-4.0-18-13-RA-HC 8/21/2014 8/21/2017 4427564XX KCFN-4.0-18-13-RA-HC 8/21/2014 8/21/2017 4427564XXX KCFN-4.0-18-13-RA-HC 8/21/2014 8/21/2017 4427566X KCFN-4.0-18-13-RA-HC 2014/03 3/1/2017 4427568X KCFN-4.0-18-13-RA-HC 2014/03 3/1/2017 4610803X KCFN-4.0-18-13-RA-HC 2014/03 3/1/2017 4954615 KCFN-4.0-18-13-RA-HC 6/1/2014 6/1/2017 5087583 KCFN-4.0-18-13-RA-HC 8/1/2014 8/1/2017 5087583X KCFN-4.0-18-13-RA-HC 8/1/2014 8/1/2017 5102705 KCFN-4.0-18-13-RA-HC 8/11/2014 8/11/2017 5102705X KCFN-4.0-18-13-RA-HC 8/11/2014 8/11/2017 5260392 KCFN-4.0-18-13-RA-HC 10/6/2014 10/6/2017 5260392X KCFN-4.0-18-13-RA-HC 10/6/2014 10/6/2017 4427454X KCFN-4.0-18-23-RA-HC 8/21/2014 8/21/2017 4427454XX KCFN-4.0-18-23-RA-HC 8/21/2014 8/21/2017 4427456X KCFN-4.0-18-23-RA-HC 2014/03 3/1/2017 4427458X KCFN-4.0-18-23-RA-HC 2014/03 3/1/2017 4667209X KCFN-4.0-18-23-R |
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Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:54 UTC. Current status: terminated.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-1390-2017%22
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