International safety notice
Urgent Field Safety Notice for Sensis, Sensis Vibe Combo, Sensis Vibe Hemo by Siemens Healthcare GmbH, Advanced Therapies Angiographie
Germany / BfArM · DEU · Jan 27, 2021
Key facts
| Title | Urgent Field Safety Notice for Sensis, Sensis Vibe Combo, Sensis Vibe Hemo by Siemens Healthcare GmbH, Advanced Therapies Angiographie |
|---|---|
| Regulator | Germany / BfArM |
| Country | DEU |
| Brand | Sensis, Sensis Vibe Combo, Sensis Vibe Hemo |
| Manufacturer | Siemens Healthcare GmbH, Advanced Therapies Angiographie |
| Models | SENSISVIBESYSTEMSWITHSOFTWAREVERSIONVD12ANDEQUIPPEDWITHHPFLEXPROͲCPCMAYSPORADICALLY, THISLETTERWILLBEDISTRIBUTEDTOAFFECTEDCUSTOMERSASUPDATEAX010, AX009, PAGE2OF2, 11007641, 11007642, SENSISVIBESYSTEMSWITHSOFTWAREVERSIONVD12ANDEQUIPPEDWITHHP, 10764561, 2019V17.04, SCF12 |
| Date | Jan 27, 2021 |
| Regulator page | bfarm.de |
At a glance
- No Recall
- No Field safety notice
- 1–9 Matching device models 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