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Arthrex, Inc. recalls K-Wire, 1.35 mm x 170 mm
Recalled May 11, 2022 · FDA recall Z-1035-2022 · Arthrex
Hazard
Products do not meet length and diameter specifications. · FDA Class II
Units
300 pieces
Sold at
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.
Description
Products do not meet length and diameter specifications.
Product
K-Wire, 1.35 mm x 170 mm
Manufacturer(s)
Arthrex, Inc.
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →