International safety notice
Verathon Medical
United Kingdom / MHRA · GBR · Jun 5, 2020
Key facts
| Title | Verathon Medical |
|---|---|
| Regulator | United Kingdom / MHRA |
| Country | GBR |
| Brand | GlideScope® Core OneTouch Cable |
| Manufacturer | Verathon Medical |
| Models | 0600-0772, REV‐00, 0800-0602, 0800-0601, ©2020, 331-2313, COVID-19, 0900-4940, LTR‐0044‐ENUK |
| Event type | Recall, Safety Notice |
| Action type | Field safety notice |
| Date | Jun 5, 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