International safety notice
Respirador Trilogy Evo (Nº producto IN2110X15B) Respirador Trilogy Evo O2 (Nº de producto ES2100X15B, IN2100X15B) Respirador Trilogy EV300 (Nº de producto IN2200X15B)
Spain / AEMPS · ESP · Sep 10, 2021
Key facts
| Title | Respirador Trilogy Evo (Nº producto IN2110X15B) Respirador Trilogy Evo O2 (Nº de producto ES2100X15B, IN2100X15B) Respirador Trilogy EV300 (Nº de producto IN2200X15B) |
|---|---|
| Regulator | Spain / AEMPS |
| Country | ESP |
| Brand | Respirador Trilogy Evo (Nº producto IN2110X15B) Respirador Trilogy Evo O2 (Nº de producto ES2100X15B, IN2100X15B) Respirador Trilogy EV300 (Nº de producto IN2200X15B) |
| Manufacturer | Respironics, EE.UU. |
| Models | 28022, 91.822.52.89, 1.06.02, CMH2O, 28050, IN2200X15B, 08908, 71515, ES2100X15B, 1.04.06, IN2100X15B, 32792 and 17 more |
| Event type | Safety Notice |
| Date | Sep 10, 2021 |
At a glance
- No Recall
- Yes Field safety notice
- 1–9 Matching device models in FDA data
- 1–9 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