International safety notice
Lasertube (Rubber) Laser resistant tracheal tube, cuffed; Endotracheal tube for laser surgery
Ireland / HPRA · IRL · Jan 7, 2020
Key facts
| Title | Lasertube (Rubber) Laser resistant tracheal tube, cuffed; Endotracheal tube for laser surgery |
|---|---|
| Regulator | Ireland / HPRA |
| Country | IRL |
| Brand | Lasertube (Rubber) Laser resistant tracheal tube, cuffed; Endotracheal tube for laser surgery |
| Manufacturer | Willy Rüsch GmbH |
| Models | 15371, 17381, 16261, 15451, 102004-000060, 15461, 17271, 14151, 15251, 14201, 18421, 18231 and 180 more |
| Event type | Recall |
| Date | Jan 7, 2020 |
| Regulator page | hpra.ie |
At a glance
- Yes Recall
- No 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