Recall StatusTerminated
Date Initiated2018-09-25
Date Terminated2020-06-04
Product Quantity9834 total
Reason for Recall
The instruction for use detail, with respect to removal of the delivery system as part of Deployment of the stent is incorrect and the IFU is being corrected to amend the instruction for use detail.
Firm Action
Urgent Medical Device Correction notification letters dated 9/25/18 were distributed to customers. The letter identified affected product, problem and actions to be taken. Urgent Medical Device Correction notification letters dated 9/25/18 were distributed to customers. Customers were instructed to:
1. Examine your inventory immediately to determine if you have affected product(s).
2. Read the notice carefully and communicate the correction to users.
3. Maintain a copy of this notice for your own records.
4. Ensure users are aware of the IFU modifications.
5. Please complete the Acknowledgement and Receipt Form within 5 business days of receiving this letter and return it via fax (812.339.7316) or email (
[email protected]).
Even if you do not have affected product(s) on hand, you must still complete the Acknowledgement and Receipt Form and return it.
6. Immediately report 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].
For questions contact Cook Medical Customer Relations at 800-457-4500 or 812-339-2235.
Root Cause
Under Investigation by firm
Distribution Pattern
US Nationwide Distribution in the states of: AK, AL, AR, AZ, CA, CO, CT, DC, FL, GA, HI, IA, ID, IL, IN, KS, KY, LA, MA, MD, ME, MI, MN, MO, MS, MT, NC, NE, NH, NJ, NV NY, OH, OK, OR, PA, RI, SC, SD, TN, TX, UT, VA, VT, WA, WI, WV, WY, and Puerto Rico.
Related FDA 510(k) Records
Devices referenced by this recall via K-numbers.
Official Source
View FDA Recall →Source: FDA Enforcement Report / Recall database. Always confirm against the official FDA record.