Arthrex, Inc.: Medical Device Recall in 2020 - (Recall #: Z-2733-2020)

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:

Sterile Low Profile Screw, Titanium, 6.7 x 65mm Part Number: AR-8967-2865S - Product Usage: is 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.

Product Classification:

Class II

Date Initiated: June 24, 2020

Date Posted: August 5, 2020

Recall Number: Z-2733-2020

Event ID: 86021

Reason for Recall:

Screws provided in packaging are 5mm shorter than intended

Status: Terminated

Product Quantity: 28 units

Code Information:

Batch Number: 10706233 UDI Number:00888867056411

Distribution Pattern:

International distribution in the countries of Denmark, United Kingdom, Sweden, Japan, Netherlands

Voluntary or Mandated:

Voluntary: Firm initiated