International safety notice
Urgent Safety Notice for THERAKOS™ UVAR XTS™ Procedural Kits, Therakos Inc.
Germany / BfArM · DEU · Mar 24, 2011
Key facts
| Title | Urgent Safety Notice for THERAKOS™ UVAR XTS™ Procedural Kits, Therakos Inc. |
|---|---|
| Regulator | Germany / BfArM |
| Country | DEU |
| Brand | THERAKOS™ UVAR XTS™ Procedural Kits, Therakos Inc. |
| Manufacturer | Urgent Safety Notice for THERAKOS™ UVAR XTS™ Procedural Kits, Therakos Inc. |
| Models | XT125, CL11-044_EU_CONFIRMATION, 01-MAR-2015, 01-MAY-2015, 09-FEB-2011, 01-FEB-2015, 01-JAN-2015, 00800, 800-828-6316, XT001, 01-APRIL-2015 |
| Date | Mar 24, 2011 |
| Regulator page | bfarm.de |
At a glance
- No Recall
- No Field safety notice
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