Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Ivoclar Vivadent IPS e.max ZirCAD CER/inLab LT A3 C17/5 - ceramic for dental use Recalled by Ivoclar Vivadent AG Due to Restorations crack during the sintering process.
What You Should Do
Stop using this product immediately. Do not consume, use, or distribute it.
Return the product to the place of purchase for a full refund. If you have questions, contact Ivoclar Vivadent AG directly.
Affected Products
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
Quantity: 639 units
Why Was This Recalled?
Restorations crack during the sintering process.
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About Ivoclar Vivadent AG
Ivoclar Vivadent AG has 4 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report