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

Recall Z-0382-2014 — Tri-Nex Healing Abutment, 0.50 mm x 5 mm height, Catalog No. HA-L-50-5. The NSI Implant System is intended to be implanted in the upper and lower jaw arches to provide support for fixed or removable dental prostheses in a single tooth, partially edentulous prostheses, or full arch prostheses. It

U.S. FDA — Device Enforcement · United States · 2013-09-13 · Class II

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Agency
U.S. FDA — Device Enforcement
Recall identifier
Z-0382-2014
Date of alert
2013-09-13
Country / jurisdiction
United States
Risk level
Class II
Risk type
recall
Brand
Southern Implants, Inc
Product category
device
Product type
Devices
Barcode (EAN/GTIN)
2676021303
Reported risk: Southern Implants is recalling the Tri-Nex healing abutment because the package was incorrectly labeled and packaged as the Tri-Nex healing abutment, 05.0 mm x 5 mm height (HA-L-50-5). The package contains the Tri-Nex healing abutment 05.0 mm x 6.0 mm Flare x 5 mm Height (HA-L-50W-5).
Primary source: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts

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