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Ivoclar Vivadent AG recalls Ivoclar Vivadent IPS e.max ZirCAD CER/inLab LT A1 C17/5 -ceramic for dental use, intended for IPS e.max ZirCAD presinter
Recalled May 13, 2020 · FDA recall Z-1837-2020 · Ivoclar Vivadent AG
Hazard
Restorations crack during the sintering process. · FDA Class II
Units
9 units
Sold at
US Nationwide distribution.
Description
Restorations crack during the sintering process.
Product
Ivoclar Vivadent IPS e.max ZirCAD CER/inLab LT A1 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: 686193
Manufacturer(s)
Ivoclar Vivadent AG
Made in
Liechtenstein
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →