International safety notice
Corrective action for Armstrong Medical Humidification Chambers and Breathing Circuits containing Humidification Chambers, Armstrong Medical Ltd.
Germany / BfArM · DEU · Nov 25, 2015
Key facts
| Title | Corrective action for Armstrong Medical Humidification Chambers and Breathing Circuits containing Humidification Chambers, Armstrong Medical Ltd. |
|---|---|
| Regulator | Germany / BfArM |
| Country | DEU |
| Brand | Armstrong Medical Humidification Chambers and Breathing Circuits containing Humidification Chambers, Armstrong Medical Ltd. |
| Manufacturer | Corrective action for Armstrong Medical Humidification Chambers and Breathing Circuits containing Humidification Chambers, Armstrong Medical Ltd. |
| Models | 120215, 270415, 140415, 240315, 250914, 160315, 161214, 220814, 304171, 250215, 240714, 071014 and 70 more |
| Date | Nov 25, 2015 |
| Regulator page | bfarm.de |
At a glance
- No Recall
- No Field safety notice
- 10–99 Matching device models in FDA data
- 10–99 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