FDA-Device2020-02-05Class II

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

Arthrex, Inc.
Hazard

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

Sold states
Nationwide in US; no distribution OUS.
Affected count
47
Manufactured in
1370 Creekside Blvd, N/A, Naples, FL, United States
Products
Arthrex Fibulock Fibular Nail Instrument Set Reusable non-sterile instruments Outrigger Targeting Guide

Official notice

https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-0919-2020

Don't want to check this manually?

We email you a Sunday digest of new federal recalls relevant to parents — free, no credit card. Or upgrade to as-it-happens alerts for the brands you actually own.

Get the Sunday Brief