International safety notice
Corrective Action for VENTIlogic LS, Weinmann
Germany / BfArM · DEU · Apr 27, 2009
Key facts
| Title | Corrective Action for VENTIlogic LS, Weinmann |
|---|---|
| Regulator | Germany / BfArM |
| Country | DEU |
| Brand | VENTIlogic LS, Weinmann |
| Manufacturer | Corrective Action for VENTIlogic LS, Weinmann |
| Models | 0-22502, 02-470, 24558, 02-100, 4940-54702-400, 040-547 |
| Date | Apr 27, 2009 |
| 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