FDA recall Z-1839-2020

Ivoclar Vivadent AG · Class II · device

Product

Ivoclar Vivadent IPS e.max ZirCAD CER/inLab LT A3 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: 686195

Reason for recall

Restorations crack during the sintering process.

Distribution

US Nationwide distribution.

Key facts

Status
Terminated
Initiation date
2020-04-13
Report date
2020-05-13
Termination date
2021-01-22
Voluntary/Mandated
Voluntary: Firm initiated
Location
Schaan, N/A, Liechtenstein

Primary source

https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-1839-2020