FDA Enforcement Class II Ongoing

SMART FLEX 6x120 BIL, 120cm The S.M.A.R.T.¿ Flex Biliary Stent System is indicated for use in the palliation of malignant strictures in the biliary tree.

Recall: Z-0217-2022 · Reported November 24, 2021

Enforcement

Recall Number
Z-0217-2022
Event ID
88821
Classification
Class II
Status
Ongoing
Product Type
Devices
Firm
Cordis Corporation
Voluntary / Mandated
Voluntary: Firm initiated
Initial Notification
Letter
Report Date
November 24, 2021
Initiation Date
October 1, 2021
Classification Date
November 12, 2021
Address
14201 NW 60th Ave, N/A, Miami Lakes, FL, 33014-2802, United States

Description

SMART FLEX 6x120 BIL, 120cm The S.M.A.R.T.¿ Flex Biliary Stent System is indicated for use in the palliation of malignant strictures in the biliary tree.

Reason

There is a potential for distal tip dislodgement or separation.

Code Info

Product Code: SF06120MB; Lot No. 266401

Distribution

US Distribution to states of: CA, FL, IN, LA, OH, OK, TX and OUS distribution to country of Canada.

Quantity

3 units