Arthrex, Inc.: Medical Device Recall in 2021 - (Recall #: Z-1310-2021)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2021.

Data Source: FDA.

Product Description:

Drill Bit, Cannulated, 5.0 mm - Product Usage: may be used in a variety of foot and ankle procedures.

Product Classification:

Class II

Date Initiated: February 24, 2021

Date Posted: April 7, 2021

Recall Number: Z-1310-2021

Event ID: 87481

Reason for Recall:

The color indicator on the proximal end of the shaft of the AR-8770-02 is the incorrect color.

Status: Terminated

Product Quantity: 9 units

Code Information:

Product Code AR-8770-02, Lot Number 032052

Distribution Pattern:

US Nationwide distribution in the states of Ohio, Oregon, Tennessee, Texas.

Voluntary or Mandated:

Voluntary: Firm initiated