FDA recall record

Bard DuaLok Breast Lesion Localization Wire, Product Code (Gauge x Length) LW0037 (20gx37mm) recall — FDA Z-2648-2014

Bard Peripheral is recalling the Bard DuaLok Breast Lesion Localization Wire because it may be at risk of having portions of the wire protruding from the…

Class IIclassification
Z-2648-2014official record ID
Sep 24, 2014report date

Recall record at a glance

Official recordZ-2648-2014
CategoryMedical Device Recalls
ClassificationClass II
FDA record statusTerminated
Recalling firmBard Peripheral Vascular Inc.
Report dateSep 24, 2014
Recall initiation dateAug 26, 2014
Quantity177,760 units
LocationTempe, AZ, United States

Official product description

Bard DuaLok Breast Lesion Localization Wire, Product Code (Gauge x Length) LW0037 (20gx37mm); LW0057 (20gx57mm), LW0077(20gx77mm), LW0107(20gx107mm), LW0137(20gx137mm). The Bard DuaLok Breast Lesion Localization Wire is intended for use as a guide for directing surgical biopsies.

Why the product was recalled

Bard Peripheral is recalling the Bard DuaLok Breast Lesion Localization Wire because it may be at risk of having portions of the wire protruding from the packaging, thus representing a breach of sterile barrier.

Distribution information

Worldwide Distribution-USA (nationwide), Australia, Canada, and European, Latin American and Asian Pacific countries.

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

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