Arthrex, Inc. recalls Arthrex Suture Anchor, Nano Corkscrew FT (consists of an anchor pre-loaded on a handled inserter including suture, with

Recalled January 23, 2019 · FDA recall Z-0724-2019 · Arthrex

Hazard

Potentially lead to anchor breakage during insertion, · FDA Class II

Units

1308 US and 110 OUS

Sold at

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

Description

Potentially lead to anchor breakage during insertion,

Product

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

Manufacturer(s)

Arthrex, Inc.

Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →