International safety notice
Teleflex
United Kingdom / MHRA · GBR · Oct 15, 2020
Key facts
| Title | Teleflex |
|---|---|
| Regulator | United Kingdom / MHRA |
| Country | GBR |
| Brand | Lasertube (Rubber) Laser resistant tracheal tube, cuffed; Endotracheal tube for laser surgery |
| Manufacturer | Teleflex |
| Models | 18491, 19161, 102004-000060, 19281, 20111, 19131, 20041, 19381, 532761, 19071, 19291, 19411 and 51 more |
| Event type | Recall, Safety Notice |
| Action type | Field safety notice |
| Date | Oct 15, 2020 |
| Regulator page | gov.uk |
At a glance
- Yes Recall
- Yes Field safety notice
- 100–999 Matching device models in FDA data
- 100–999 Matching catalog numbers in FDA data
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