FDA recall record

Medtronic Sofamor Danek Usa, Inc - Dallas Tool Legend 16cm 2.4 mm wire pass for Midas Rex recall — FDA Z-0321-2016

The wire pass hole is not present on the tools.

Class IIclassification
Z-0321-2016official record ID
Dec 2, 2015report date

Recall record at a glance

Official recordZ-0321-2016
CategoryMedical Device Recalls
ClassificationClass II
FDA record statusTerminated
Recalling firmMedtronic Sofamor Danek Usa, Inc - Dallas Distribution
Report dateDec 2, 2015
Recall initiation dateOct 21, 2015
Quantity9 pieces
LocationHaltom City, TX, United States

Official product description

Tool Legend 16cm 2.4 mm wire pass for Midas Rex Legend Dissecting Tool. Used by surgeons to drill holes.

Why the product was recalled

The wire pass hole is not present on the tools.

Distribution information

Distributed in the states of California, New York, and Texas and the country of Belgium.

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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