International safety notice
Flexicare Medical
United Kingdom / MHRA · GBR · Oct 18, 2019
Key facts
| Title | Flexicare Medical |
|---|---|
| Regulator | United Kingdom / MHRA |
| Country | GBR |
| Brand | BriteBlade Pro Single Use Fibre Optic Blade & BritePro Solo Single Use Fibre Optic Laryngoscope |
| Manufacturer | Flexicare Medical |
| Models | 181200353, 180900401, 180900316, 2019-001, 181100290, 181100301, 190100335, 181100289, 040-713, 180901083, 181201031, 180802595 and 4 more |
| Event type | Recall, Safety Notice |
| Action type | Field safety notice |
| Date | Oct 18, 2019 |
| 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