International safety notice
Corrective measure for AXIOM / Artis zee in conjunction with a wireless foot switch, Siemens Healthcare
Germany / BfArM · DEU · Jan 17, 2012
Key facts
| Title | Corrective measure for AXIOM / Artis zee in conjunction with a wireless foot switch, Siemens Healthcare |
|---|---|
| Regulator | Germany / BfArM |
| Country | DEU |
| Brand | AXIOM / Artis zee in conjunction with a wireless foot switch, Siemens Healthcare |
| Manufacturer | Corrective measure for AXIOM / Artis zee in conjunction with a wireless foot switch, Siemens Healthcare |
| Models | 7728350, 5904466, 4787805, AX044, 5904649, 7008605, 5917054, 4787898, 5904441, 7412807, 4787813, 5904656 and 20 more |
| Date | Jan 17, 2012 |
| Regulator page | bfarm.de |
At a glance
- No Recall
- No Field safety notice
- 10–99 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