Arthrex, Inc.: Medical Device Recall in 2022 - (Recall #: Z-1035-2022)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2022.

Data Source: FDA.

Product Description:

K-Wire, 1.35 mm x 170 mm

Product Classification:

Class II

Date Initiated: March 25, 2022

Date Posted: May 11, 2022

Recall Number: Z-1035-2022

Event ID: 89984

Reason for Recall:

Products do not meet length and diameter specifications.

Status: Ongoing

Product Quantity: 300 pieces

Code Information:

Part Number: AR-8610K-43, Batch 1298116640 UDI: 00888867197084

Distribution Pattern:

Worldwide distribution - US Nationwide distribution in the states of OH, TN, MO, LA, IA, AZ, PA, NY, OR and the countries of to Belgium, Egypt, Finland, France, Germany, Italy, Netherlands, Norway, Poland, Portugal, and Spain.

Voluntary or Mandated:

Voluntary: Firm initiated