International safety notice
Corrective action for Acrobat V & SUV Vacuum Off-Pump Systems and Xpose 3 & 4 Access Devices, Maquet
Germany / BfArM · DEU · Aug 21, 2014
Key facts
| Title | Corrective action for Acrobat V & SUV Vacuum Off-Pump Systems and Xpose 3 & 4 Access Devices, Maquet |
|---|---|
| Regulator | Germany / BfArM |
| Country | DEU |
| Brand | Acrobat V & SUV Vacuum Off-Pump Systems and Xpose 3 & 4 Access Devices, Maquet |
| Manufacturer | Corrective action for Acrobat V & SUV Vacuum Off-Pump Systems and Xpose 3 & 4 Access Devices, Maquet |
| Models | 25098402, 25071619, OM-9100S, 25088336, 25094473, 25081363, 25084722, 25062341, 25072852, 25064428, 25085850, 25093619 and 178 more |
| Date | Aug 21, 2014 |
| Regulator page | bfarm.de |
At a glance
- No Recall
- No Field safety notice
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