Product Wiki · Recalls · U.S. FDA — Device Enforcement

Conical 17 degree Angled Abutment Dental implants — recall Z-2504-2016

U.S. FDA — Device Enforcement · United States · 2015-11-25 · Class II

As described by U.S. FDA — Device Enforcement: Conical 17 degree Angled Abutment Dental implants

Compiled from an official source — the facts on this page are reproduced from the issuing authority’s own published notice, which is linked above. No AI-generated text appears on this page. How we use AI →
Agency
U.S. FDA — Device Enforcement
Recall identifier
Z-2504-2016
Date of alert
2015-11-25
Country / jurisdiction
United States
Risk level
Class II
Risk type
recall
Brand
Biomet 3i, LLC
Product category
device
Product type
Devices
Recall status
Terminated — the recall action is complete and the FDA has closed it
Initiated by
Voluntary: Firm initiated
Distribution
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, Germa
Reported risk: Pouches may not have been sealed during packing.
Primary source: https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?start_search=1&

Verify each fact at the issuing agency before acting. Recall scope, affected lots, and remediation instructions may be updated by the agency after our last sync.

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