FDA recall record

C.R. Bard BARD INLAY Ureteral Stent with Suture, Manufacturer: C.R recall — FDA Z-0404-2017

Labeling: Statement was added to the Warnings/Precautions section requesting end users to consider the presence of a knot if significant resistance is…

Class IIclassification
Z-0404-2017official record ID
Nov 23, 2016report date

Recall record at a glance

Official recordZ-0404-2017
CategoryMedical Device Recalls
ClassificationClass II
FDA record statusTerminated
Recalling firmC.R. Bard, Inc.
Report dateNov 23, 2016
Recall initiation dateOct 13, 2016
Quantity75,089 units
LocationCovington, GA, United States

Official product description

BARD INLAY Ureteral Stent with Suture, Manufacturer: C.R. Bard, Inc., Covington, GA 30014.

Why the product was recalled

Labeling: Statement was added to the Warnings/Precautions section requesting end users to consider the presence of a knot if significant resistance is encountered during attempts at removal.

Distribution information

U.S. Nationwide.

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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