International safety notice
Covidien DAR™ airway products
Ireland / HPRA · IRL · May 5, 2021
Key facts
| Title | Covidien DAR™ airway products |
|---|---|
| Regulator | Ireland / HPRA |
| Country | IRL |
| Brand | Covidien DAR™ airway products |
| Manufacturer | Covidien llc |
| Models | 20D0652FAX, 19E1566FAX, 19B1488FAX, 18M0943FAX, 20L1073FAX, 20J0102FAX, 20F1148FAX, 20D0430FAX, 20C0870FAX, 20C0291FAX, 20G1363FAX, 20A0681FAX and 8042 more |
| Event type | Recall |
| Date | May 5, 2021 |
| Regulator page | hpra.ie |
At a glance
- Yes Recall
- No Field safety notice
- 10–99 Matching device models in FDA data
- 10–99 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