International safety notice
Mucosal Atomization Device (MAD)
Ireland / HPRA · IRL · Nov 2, 2016
Key facts
| Title | Mucosal Atomization Device (MAD) |
|---|---|
| Regulator | Ireland / HPRA |
| Country | IRL |
| Brand | Mucosal Atomization Device (MAD) |
| Manufacturer | Teleflex Medical |
| Models | 160800, 160125, 160804, 160440, 160523, 160718, 160126, 160107, 160117, 160400, 160801, 160518 and 67 more |
| Event type | Recall |
| Date | Nov 2, 2016 |
| 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