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

BIOMET 3i CERTAIN LOW PROFILE ONE-PIECE ABUTMENT 3.4MM(D) X 2MM(H) 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 — recall Z-0836-2017

U.S. FDA — Device Enforcement · United States · 2016-09-14 · Class II

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Agency
U.S. FDA — Device Enforcement
Recall identifier
Z-0836-2017
Date of alert
2016-09-14
Country / jurisdiction
United States
Risk level
Class II
Risk type
recall
Brand
Biomet 3i, LLC
Product category
device
Product type
Devices
Barcode (EAN/GTIN)
2016020057
Reported risk: A limited number of product pouches may not have been sealed during packaging.
Primary source: https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?start_search=1&

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