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Biomet 3i, LLC recalls BIOMET 3i LOW PROFILE ABUTMENT NON-HEXED TEMPORARY CYLINDER An endosseous dental implant abutment is a premanufacture
Recalled December 28, 2016 · FDA recall Z-0861-2017 · Biomet 3i
Hazard
A limited number of product pouches may not have been sealed during packaging. · FDA Class II
Units
1,371
Sold at
Worldwide Distribution to Austria, Belgium, Switzerland, Germany, Spain, France, Great Britain, Ireland, Italy, Lithuania, Portugal and Sweden
Description
A limited number of product pouches may not have been sealed during packaging.
Product
BIOMET 3i LOW PROFILE ABUTMENT NON-HEXED TEMPORARY CYLINDER An endosseous dental implant abutment is a premanufactured prosthetic component directly connected to the endosseous dental implant and is intended for use as an aid in prosthetic rehabilitation
Manufacturer(s)
Biomet 3i, LLC
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →