FDA Recall Terminated

Cook Celect PlatinumVena Cava Filter Set Catalog Number/GPN: IGTCFS-65-1-FEM-CELECT-PT G34502; IGTCFS-65-1-JUG-CELECT-PT G34309; IGTCFS-65-1-UNI-CELECT-PT G34505;

Recall: Z-0876-2022 · Initiated February 14, 2022

Recall

Recall Number
Z-0876-2022
Event Number
89689
Firm
Cook Medical Incorporated
FEI Number
3005580113
Product Code
DTK
Status
Terminated
Root Cause
Labeling design
Initiated
February 14, 2022
Terminated
November 7, 2024
Address
400 N Daniels Way, Bloomington, IN, 47404-9155

Description

Cook Celect PlatinumVena Cava Filter Set Catalog Number/GPN: IGTCFS-65-1-FEM-CELECT-PT G34502; IGTCFS-65-1-JUG-CELECT-PT G34309; IGTCFS-65-1-UNI-CELECT-PT G34505;

Reason

IFU update includes an update to the Device description, Intended Use/Indications for Use, Contraindications, Warnings, Precautions, Potential adverse events

Action

Cook issued Urgent Medical Device Correction letter on February 14, 2022 via courier to US consignees. Letter states reason for recall, health risk and action to take: 1. Please read the new IFU in entirety. 2. The electronic versions of the IFUs can be found on the Cook Medical website by Catalogue Number (RPN): https://ifu.cookmedical.com/ifuPub/searchIfu.jsf 3. Your Cook Medical Sales Representative can facilitate delivery of new IFUs for your inventory upon request. 4. Please complete and return the Acknowledgement and Receipt Form within 5 business days of receiving this letter regardless of whether you have affected product(s) on hand. You may return the Form via fax (812.339.7316) or email ([email protected]). 5. Please continue to report any adverse events to Cook Medical Customer Relations by phone at 800.457.4500 or 812.339.2235, Monday through Friday between 7:30 am and 5:00 pm (Eastern Time) or by email to [email protected]. 6. Adverse events or quality problems experienced with the use of this product may also be reported to the FDA. Visit http://www.fda.gov/Safety/MedWatch/HowToReport/default.htm to obtain a form to fax or mail or call the FDA at 800.FDA.1088. This notice must be shared with appropriate personnel, including down to the user level, within your organization or with any organization where the potentially affected devices may have been transferred. If you have any questions or concerns, please contact Cook Medical Customer Relations at 800.457.4500 or 812.339.2235

Distribution

US Nationwide - Worldwide Distribution Foreign: Canada, Bahamas ,Chile Guam

Quantity

52,590 units