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

Recall Z-1838-2020 — Ivoclar Vivadent IPS e.max ZirCAD CER/inLab LT A2 C17/5 - ceramic for dental use,intended for IPS e.max ZirCAD presintered yttrium oxide-stabilized zirconium oxide blocks for the CAD/ CAM technology Product Number: 686194

U.S. FDA — Device Enforcement · Liechtenstein · 2020-04-13 · Class II

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Agency
U.S. FDA — Device Enforcement
Recall identifier
Z-1838-2020
Date of alert
2020-04-13
Country / jurisdiction
Liechtenstein
Risk level
Class II
Risk type
recall
Brand
Ivoclar Vivadent AG
Product category
device
Product type
Devices
Reported risk: Restorations crack during the sintering process.
Primary source: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts

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