IPS e.max ZirCAD 758434Recalls & reported problems
Ivoclar Vivadent Aktiengesellschaft · IPS e.max ZirCAD CER/in.Prime BL1 C17/3 · Class 2
All models of IPS e.max ZirCAD (6)
Data updated Oct 16, 2026 from official FDA records · Editorial policy
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. What reports can and can't tell you · How this data works · Data updated Oct 16, 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-1703-2024 · Root cause: Under Investigation by firm · Recall details · FDA record ↗
Other POWDER, PORCELAIN devices
- IPS e.max ZirCAD 758441Ivoclar 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 758439Ivoclar Vivadent Aktiengesellschaft · POWDER, PORCELAIN1 recall0 reports
- NexxZr® T Multi / W-98-16-NT-A350-MT 745451Sagemax Bioceramics, Inc · Powder, Porcelain1 recall0 reports
- IPS e.max ZirCAD 758438Ivoclar Vivadent Aktiengesellschaft · POWDER, PORCELAIN1 recall0 reports
- IPS e.max ZirCAD 758437Ivoclar Vivadent Aktiengesellschaft · POWDER, PORCELAIN1 recall0 reports
- Ceramill® Zolid Zolid fx ML D2/D3 98x20 NAmann Girrbach AG · Powder, Porcelain1 report
Sources and updates
- Device record: FDA GUDID, file dated Oct 13, 2026 · View this device in AccessGUDID ↗
- Adverse event reports: FDA MAUDE, file dated Oct 14, 2026
- Recalls: FDA Medical Device Recalls, file dated Oct 16, 2026 · each recall links to the FDA recall notice
- Page last rebuilt: Oct 16, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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