FDA-Device2016-08-24Class II
Preformance Temporary Cylinder Dental implants
Biomet 3i, LLC
Hazard
Pouches may not have been sealed during packing.
Sold states
Worldwide Distribution Nationwide andHawaii, Guam, Puerto Rico and Virgin Islands (U.S.) . FOREIGN CONSIGNEES: Albania, Andorra, Argentina, Australia, Austria, Barbados, Belgium, Bolivia, Brazil, Canada, Cayman Islands, Chile, China, Colombia, Costa Rica, Denmark, Dominican Republic, France, Germany, Great Britain, Greece, Hong Kong, Hungary, India, Ireland, Israel, Italy, Jamaica, Japan, Korea (South), Kuwait, Lebanon, Liechtenstein, Lithuania, Martinique, Mexico, Mongolia, Netherlands, Northern Mariana Islands, Paraguay, Peru, Poland, Portugal, Qatar, Reunion, Russian Federation, Saudi Arabia, Singapore, Slovenia, South Africa, Spain, Sweden, Switzerland, Syria, Taiwan, Thailand, Trinidad and Tabago, Turkey, United Arab Emirates, Uruguay and Viet Nam.
Affected count
1,648,273 devices (all products subject to this recall)
Manufactured in
4555 Riverside Dr, N/A, Palm Beach Gardens, FL, United States
Products
Preformance Temporary Cylinder Dental implants
Official notice
https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-2437-2016Don't want to check this manually?
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