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Biomet 3i, LLC recalls 3I OSSEOTITE CERTAIN DENTAL IMPLANTS, 4x11.5 mm, Sterile, Rx only.
Recalled September 28, 2016 · FDA recall Z-2845-2016 · Biomet 3i
Hazard
Product was incorrectly packaged. · FDA Class II
Units
92 units
Sold at
US Distributions to the states of : CA and FL., and Worldwide to : Colombia, France, Germany, Italy, and Spain.
Description
Product was incorrectly packaged.
Product
3I OSSEOTITE CERTAIN DENTAL IMPLANTS, 4x11.5 mm, Sterile, Rx only.
Manufacturer(s)
Biomet 3i, LLC
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →