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Arthrex, Inc. recalls Arthrex Suture Washer
Recalled October 12, 2016 · FDA recall Z-2918-2016 · Arthrex
Hazard
The device was assembled incorrectly. Suture and washer were not assembled; components were placed loose in the package. · FDA Class III
Units
45 devices
Sold at
OR, NY, MN, KY, CA, ID, CO, MA, and FL. Thailand.
Description
The device was assembled incorrectly. Suture and washer were not assembled; components were placed loose in the package.
Product
Arthrex Suture Washer
Manufacturer(s)
Arthrex, Inc.
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →