Ivoclar Vivadent recalls IPS e.max ZirCAD CER/inLab Start.Kit LT ceramic for dental use due to restorations cracking during sintering. Affected units have specific product numbers and lot numbers.
Restorations crack during the sintering process.
Ivoclar Vivadent is recalling IPS e.max ZirCAD CER/inLab Start.Kit LT ceramic for dental use because restorations can crack during the sintering process. This could lead to dental issues if the ceramic pieces break during use.
The ceramic material can crack during the sintering process, which is when the material is heated to fuse it into a final shape. This cracking could cause the restoration to break, potentially leading to dental problems for patients.
Dentists and dental labs using the recalled ceramic kit are most at risk. Patients receiving restorations made from this kit may experience issues if the ceramic cracks.
Check for product number 686282EN and lot numbers Z0007Z, Z000KK, Y49356, or Z006HV on the kit packaging. The kit is intended for IPS e.max ZirCAD dental restorations.
Look for product number 686282EN and lot numbers Z0007Z, Z000KK, Y49356, or Z006HV on the kit packaging.
The kit can cause restorations to crack during the sintering process, which may lead to dental issues.
Check the product number and lot numbers on the packaging to see if it's affected. If it is, contact Ivoclar Vivadent for further instructions.
The recall record does not mention a fix or remedy for this issue.
We’ve drafted a message you can send Ivoclar Vivadent to request your refund or repair — edit it as you like.
Subject: Recall Z-1840-2020 — Ivoclar Vivadent Ivoclar Vivadent Hello, I own a Ivoclar Vivadent that is covered by recall Z-1840-2020 from Ivoclar Vivadent. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
Experiences, tips, and questions from readers. Every comment is reviewed before it appears.
No comments yet — be the first to share your experience.
The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.