International safety notice
Aesculap - B Braun
United Kingdom / MHRA · GBR · Nov 19, 2020
Key facts
| Title | Aesculap - B Braun |
|---|---|
| Regulator | United Kingdom / MHRA |
| Country | GBR |
| Brand | Aesculap Univation X System |
| Manufacturer | Aesculap - B Braun |
| Models | N0714, N0713, 01.10.2020, N0721, N0723, SA-DE13-M-5-4-02-000-5-A-EN, N0715, N0712, N0722, N0711, 7461-95 |
| Event type | Recall, Safety Notice |
| Action type | Field safety notice |
| Date | Nov 19, 2020 |
| Regulator page | gov.uk |
At a glance
- Yes Recall
- Yes 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