FDA recall record

Cordis SMART FLEX 10x100 BIL, 120cm The S.M.A.R.T.¿ Flex Biliary Stent System is indicated recall — FDA Z-0221-2022

There is a potential for distal tip dislodgement or separation.

Class IIclassification
Z-0221-2022official record ID
Nov 24, 2021report date

Recall record at a glance

Official recordZ-0221-2022
CategoryMedical Device Recalls
ClassificationClass II
FDA record statusOngoing
Recalling firmCordis Corporation
Report dateNov 24, 2021
Recall initiation dateOct 1, 2021
Quantity4 units
LocationMiami Lakes, FL, United States

Official product description

SMART FLEX 10x100 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.

Why the product was recalled

There is a potential for distal tip dislodgement or separation.

Distribution information

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

How to read the classification

FDA Class II indicates a situation in which use of or exposure to the product may cause temporary or medically reversible adverse health consequences, or where the probability of serious consequences is remote. The classification shown here comes from the FDA record.

Additional record details

Recall type: Voluntary: Firm initiated. Initial notification: Letter.

What to do next

If you believe you have the recalled product, use the recall number and firm information above to confirm the official notice and follow the instructions issued by the FDA, recalling firm, retailer or product manufacturer. For drugs and medical devices, decisions about treatment or medical care should be discussed with a qualified health professional.

About this record

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