International safety notice
Safety Information about handling problems with both adapters for the extension device 1150.59AC, MAQUET GmbH
Germany / BfArM · DEU · May 22, 2014
Key facts
| Title | Safety Information about handling problems with both adapters for the extension device 1150.59AC, MAQUET GmbH |
|---|---|
| Regulator | Germany / BfArM |
| Country | DEU |
| Brand | the extension device 1150.59AC, MAQUET GmbH |
| Manufacturer | Safety Information about handling problems with both adapters for the extension device 1150.59AC, MAQUET GmbH |
| Models | 1150.59AC, DE35660400180250230000, 144021332, 3115.2469, 932-19672, 39487, 932-672, D-76437, 29420, COBADEFF665, 932-868, 250230000 and 3 more |
| Date | May 22, 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