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Zimmer Biomet, Inc. recalls Dual Mobility Vivacit-E Bearing, Model Number 110031009
Recalled October 14, 2020 · FDA recall Z-0057-2021 · Zimmer Biomet
Hazard
The outer package is labeled as a Size C 38 mm, however, the implant inside the package is a Size E 42 mm. · FDA Class II
Units
31
Sold at
Products were distributed to the following US states: FL, ID, IL, IN, KY, MA, MD, MI, MN, NC, NJ, OH, OR, PA, SC, TX, UT, VA, WI, and WV.
Description
The outer package is labeled as a Size C 38 mm, however, the implant inside the package is a Size E 42 mm.
Product
Dual Mobility Vivacit-E Bearing, Model Number 110031009
Manufacturer(s)
Zimmer Biomet, Inc.
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →