Arthrex, Inc.: Medical Device Recall in 2019 - (Recall #: Z-0724-2019)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2019.

Data Source: FDA.

Product Description:

Arthrex Suture Anchor, Nano Corkscrew FT (consists of an anchor pre-loaded on a handled inserter including suture, with needles.) Part Number AR-1317FT Product Usage: Soft tissue fixation to bone in the hand and wrist

Product Classification:

Class II

Date Initiated: November 19, 2018

Date Posted: January 23, 2019

Recall Number: Z-0724-2019

Event ID: 81819

Reason for Recall:

Potentially lead to anchor breakage during insertion,

Status: Ongoing

Product Quantity: 1308 US and 110 OUS

Code Information:

Lots #: 10175216, 1075219, 10199557, and 10199558

Distribution Pattern:

Worldwide Distribution - US Nationwide in the states of AL, AR, AZ, CA, CO, CT, DC, FL, GA, HI, IA, ID, IL, IN, KS, KY, LA, MA, MD, ME, MI, MN, MO, MS, NC, ND, NE, NH, NJ, NV, OH, OK, OR, PA, RI, SC, SD, TN, TX, UT, VA, VT, WA, WI, and WV and the countries of Finland and Germany

Voluntary or Mandated:

Voluntary: Firm initiated