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

Recall Z-2440-2016 — Provide Impression Coping Dental implants

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

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Agency
U.S. FDA — Device Enforcement
Recall identifier
Z-2440-2016
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
Reported risk: Pouches may not have been sealed during packing.
Primary source: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts

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