Arthrex, Inc. recalls K-Wire, 1.35 mm x 170 mm
- Recall date
- March 25, 2022
- Source
- U.S. Food & Drug Administration (FDA) — enforcement report
- Recall number
- Z-1035-2022
- FDA classification
- Class II
- Brand / firm
- Arthrex, Inc.
- Sold / distributed
- 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.
Why it was recalled
Products do not meet length and diameter specifications.
Class II means using this product may cause temporary or medically reversible health problems; the chance of serious harm is remote.
What was recalled
K-Wire, 1.35 mm x 170 mm
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