International safety notice
Lombard Medical
United Kingdom / MHRA · GBR · Jun 30, 2017
Key facts
| Title | Lombard Medical |
|---|---|
| Regulator | United Kingdom / MHRA |
| Country | GBR |
| Brand | Altura Endograft System |
| Manufacturer | Lombard Medical |
| Models | 01-AA-24-090 |
| Event type | Safety Notice |
| Action type | Field safety notice |
| Date | Jun 30, 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