Reported Aug 5, 2020 · Terminated

Sterile Low Profile Screw, Titanium, 6.7 x 65mm Part Number: AR-8967-2865S - Product Usage: is intended to be used as a…

Arthrex, Inc.

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

What you should do

Stop using the affected lot and contact the recalling firm for the return or refund process. Check the FDA enforcement report for lot-level detail.

Firm contact: Arthrex, Inc. · 1370 Creekside Blvd · Naples, FL · 34108-1945

Is this the product you have?

  • Sterile Low Profile Screw, Titanium, 6.7
  • x 65mm Part NumberAR-8967-2865S -
  • Product Usageis intended to be used as a stand-alone bone screw, or in a plate-screw system for internal bone fixation for bone fractures, fusions, osteotomies and non-unions
Lot codes and dates
  • Batch Number10706233
  • UDI Number00888867056411
Amount recalled
28 units

Why it was recalled

Screws provided in packaging are 5mm shorter than intended

This product could cause temporary or reversible health problems — stop using it.

Want the full recall guide?

The guide adds the identifying codes laid out for scanning, symptoms to watch for, a timeline, and news coverage of this recall.

Free recall alerts

Get alerted about new Arthrex, Inc. recalls

One email when a matching recall is published. No account, no cost, unsubscribe in one click.

Where this came from

Source: U.S. Food & Drug Administration (openFDA)

Read the FDA (openFDA device enforcement) notice

Notice updated Feb 16, 2021 · Data as of Sep 19, 5:29 PM UTC

RecallNow is not a government agency. Every fact on this page is published by the FDA, USDA or CPSC and links back to their notice.