International safety notice

Batch recall of OptraPol / Tetric N-Ceram System Kit A2/N Univ. 6g / Telio CS C&B Starter Kit A2 / Direct Restoratives Workshop Kit / Composite Workshop Kit (Emp. Bulk Fill), lvoclar Vivadent AG

Germany / BfArM · DEU · Jul 6, 2016

Key facts

Title Batch recall of OptraPol / Tetric N-Ceram System Kit A2/N Univ. 6g / Telio CS C&B Starter Kit A2 / Direct Restoratives Workshop Kit / Composite Workshop Kit (Emp. Bulk Fill), lvoclar Vivadent AG
Regulator Germany / BfArM
Country DEU
Brand Batch recall of OptraPol / Tetric N-Ceram System Kit A2/N Univ. 6g / Telio CS C&B Starter Kit A2 / Direct Restoratives Workshop Kit / Composite Workshop Kit (Emp. Bulk Fill), lvoclar Vivadent AG
Manufacturer Batch recall of OptraPol / Tetric N-Ceram System Kit A2/N Univ. 6g / Telio CS C&B Starter Kit A2 / Direct Restoratives Workshop Kit / Composite Workshop Kit (Emp. Bulk Fill), lvoclar Vivadent AG
Models UL0838, 634463, V19573, 680184AN, V20567, 634462, VL0704, UL0843, 634458, NO.6344663, 634459, TRAP01 and 9 more
Date Jul 6, 2016
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

Browse all International device safety notices