International safety notice
Recall of Spinocath G24/G29 and G22/G27, B. Braun Melsungen AG
Germany / BfArM · DEU · Sep 29, 2016
Key facts
| Title | Recall of Spinocath G24/G29 and G22/G27, B. Braun Melsungen AG |
|---|---|
| Regulator | Germany / BfArM |
| Country | DEU |
| Brand | Recall of Spinocath G24/G29 and G22/G27, B. Braun Melsungen AG |
| Manufacturer | Recall of Spinocath G24/G29 and G22/G27, B. Braun Melsungen AG |
| Models | 05661, 71-XXXX, 42690900, 75-XXXX, 34209, 4517725, 34212, 4517717, 2016-09-15 |
| Date | Sep 29, 2016 |
| 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