FDA Enforcement
Class II
Terminated
Zilver 518 Biliary Stent 4mm x 20mm, Catalog Number: ZIB5-125-4.0-20 Product Usage: The Zilver 518 and 635 Biliary Stents are intended for palliation of malignant neoplasms in the biliary tree.
Recall: Z-0314-2019
·
Reported November 7, 2018
Enforcement
- Recall Number
- Z-0314-2019
- Event ID
- 81238
- Classification
- Class II
- Status
- Terminated
- Product Type
- Devices
- Firm
- Cook Medical Incorporated
- Voluntary / Mandated
- Voluntary: Firm initiated
- Initial Notification
- Letter
- Report Date
- November 7, 2018
- Initiation Date
- September 25, 2018
- Classification Date
- October 31, 2018
- Termination Date
- June 4, 2020
- Address
- 400 N Daniels Way, N/A, Bloomington, IN, 47404-9155, United States
Description
Zilver 518 Biliary Stent 4mm x 20mm, Catalog Number: ZIB5-125-4.0-20 Product Usage: The Zilver 518 and 635 Biliary Stents are intended for palliation of malignant neoplasms in the biliary tree.
Reason
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.
Code Info
GPN: G31437
Distribution
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.
Quantity
9834 total