IPS e.max ZirCAD 758439Recalls & reported problems
Ivoclar Vivadent Aktiengesellschaft · IPS e.max ZirCAD CER/in.Prime A3 C17/5 · Class 2
1 open recall names this device. See the recall details and contact the manufacturer or your healthcare provider.
- Adverse event reports
- 0
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 1
Summary
No MAUDE adverse event reports in our data reference this device identifier directly.
1 FDA recall record name this device's identifier, 1 still open.
Reports come from manufacturers, hospitals and patients and are not verified by the FDA. A report does not prove the device caused the event, and counts can't be used to compare devices or estimate failure rates. How this data works · Data updated Oct 13, 2026.
Recalls naming this device
- Apr 5, 2024Open, Classified
Defective blocks may show cracks after sintering If cracks are unnoticed, restorations may fracture in the patient's mouth and require restoration
Z-1706-2024 · Root cause: Under Investigation by firm · FDA record ↗
Other POWDER, PORCELAIN devices
- IPS e.max ZirCAD 758438Ivoclar Vivadent Aktiengesellschaft · POWDER, PORCELAIN1 recall0 reports
- IPS e.max ZirCAD 758437Ivoclar Vivadent Aktiengesellschaft · POWDER, PORCELAIN1 recall0 reports
- IPS e.max ZirCAD 758443Ivoclar Vivadent Aktiengesellschaft · POWDER, PORCELAIN1 recall0 reports
- Straumann® Variobase® Abutments and Straumann® n!ce® Zirconia discs Bridges (tooth borne)Institut Straumann AG · POWDER, PORCELAIN1 recall0 reports
- IPS e.max ZirCAD 758434Ivoclar Vivadent Aktiengesellschaft · POWDER, PORCELAIN1 recall0 reports
- IPS e.max ZirCAD 758441Ivoclar Vivadent Aktiengesellschaft · POWDER, PORCELAIN1 recall0 reports
- NexxZr® T Multi / W-98-16-NT-A350-MT 745451Sagemax Bioceramics, Inc · Powder, Porcelain1 recall0 reports
- Ceramill® Zolid Zolid fx ML D2/D3 98x20 NAmann Girrbach AG · Powder, Porcelain1 report
Sources: FDA GUDID, MAUDE and Medical Device Recalls via openFDA. openFDA data is not validated for clinical or regulatory use.