International safety notice
Corrective action for IPS e.max Ceram and related products, Ivoclar Vivadent AG
Germany / BfArM · DEU · Jun 23, 2015
Key facts
| Title | Corrective action for IPS e.max Ceram and related products, Ivoclar Vivadent AG |
|---|---|
| Regulator | Germany / BfArM |
| Country | DEU |
| Brand | IPS e.max Ceram and related products, Ivoclar Vivadent AG |
| Manufacturer | Corrective action for IPS e.max Ceram and related products, Ivoclar Vivadent AG |
| Models | U11702, 635528DN, 597041, 650G1, U16100, U18858, T43549, 634609, U01578, 596836AN, 605474EN, 596837AN and 28 more |
| Date | Jun 23, 2015 |
| Regulator page | bfarm.de |
At a glance
- No Recall
- No Field safety notice
- 1–9 Matching device models in FDA data
- 1–9 Matching catalog numbers in FDA data
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About International device safety notices
Field safety notices, recalls and safety alerts published by about 30 national medical device regulators outside the United States, matched by Orca1 to FDA device data.
Source: National medical device regulators (as listed), compiled by Orca1