Arthrex, Inc.: Medical Device Recall in 2020 - (Recall #: Z-0919-2020)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2020.

Data Source: FDA.

Product Description:

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

Product Classification:

Class II

Date Initiated: December 17, 2019

Date Posted: February 5, 2020

Recall Number: Z-0919-2020

Event ID: 84594

Reason for Recall:

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

Status: Terminated

Product Quantity: 47

Code Information:

Batch/Lot 051838

Distribution Pattern:

Nationwide in US; no distribution OUS.

Voluntary or Mandated:

Voluntary: Firm initiated