International safety notice
Brainlab AG
United Kingdom / MHRA · GBR · Nov 16, 2017
Key facts
| Title | Brainlab AG |
|---|---|
| Regulator | United Kingdom / MHRA |
| Country | GBR |
| Brand | Brainlab Navigation System Spine & Trauma 3D |
| Manufacturer | Brainlab AG |
| Models | 19154-03, 19154-04 |
| Event type | Safety Notice |
| Action type | Field safety notice |
| Medical specialty | Anaesthetics, Cardiology, Care home staff, Cosmetic surgery, Critical care, General practice, Haematology and oncology, Infection prevention, Obstetrics and gynaecology, Orthopaedics, Paediatrics, Pharmacy, Physiotherapy and occupational therapy, Renal medicine, Theatre practitioners, Vascular and cardiac surgery |
| Date | Nov 16, 2017 |
| Regulator page | gov.uk |
At a glance
- No 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