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Zimmer, Inc. recalls VER2 HANDLE, PIN REWORK, RT Nonsterile
Recalled August 20, 2014 · FDA recall Z-2229-2014 · Zimmer
Hazard
The firm received complaints for failure of the handle to remain assembled to the rasp during use due to various failure modes, including fracture of the leaf spring. · FDA Class II
Units
412 units
Sold at
Worldwide Distribution-USA (nationwide) including the states of AK, AL, AZ, CA, CO, FL, GA, IN, KS, KY, MI, MN, NC, NJ, NY, OH, OK, OR, PA, SD, TN, TX, UT, and VA, and the countries of Australia, France, Germany, Italy, Switzerland, and Canada.
Description
The firm received complaints for failure of the handle to remain assembled to the rasp during use due to various failure modes, including fracture of the leaf spring.
Product
VER2 HANDLE, PIN REWORK, RT Nonsterile
Manufacturer(s)
Zimmer, Inc.
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →