medical Class II Updated 2020-02-05

Arthrex, Inc. recalls Arthrex Fibulock Fibular Nail Instrument Set Reusable non-s

Recalled Product

Arthrex Fibulock Fibular Nail Instrument Set Reusable non-sterile instruments Outrigger Targeting Guide

Hazard / Issue

There is a potential for blockage of the Hub Attachment Tube.

Issued by

FDA

Distribution: Nationwide (United States)
Lot/Code Info: Batch/Lot 051838
View official government recall

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