International safety notice
Recall for the ProAQT-Sensor, PULSION Medical Systems SE
Germany / BfArM · DEU · Nov 12, 2014
Key facts
| Title | Recall for the ProAQT-Sensor, PULSION Medical Systems SE |
|---|---|
| Regulator | Germany / BfArM |
| Country | DEU |
| Brand | the ProAQT-Sensor, PULSION Medical Systems SE |
| Manufacturer | Recall for the ProAQT-Sensor, PULSION Medical Systems SE |
| Models | 14EK20, DE204234444, 13KD13, 14BDIO, 192563, 15187967, PV8810, 85622, 89459914-0, 0-85622, 70020270, CAPA-2014-034 and 11 more |
| Date | Nov 12, 2014 |
| 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