International safety notice
Corrective action for various products for inhalation therapy, Teleflex Medical
Germany / BfArM · DEU · Feb 25, 2015
Key facts
| Title | Corrective action for various products for inhalation therapy, Teleflex Medical |
|---|---|
| Regulator | Germany / BfArM |
| Country | DEU |
| Brand | inhalation therapy, Teleflex Medical |
| Manufacturer | Corrective action for various products for inhalation therapy, Teleflex Medical |
| Models | 039147, 470137, 052136, 490137, 217147, 289147, 569137, 124147, 155136, 043147, 033147, 060147 and 1248 more |
| Date | Feb 25, 2015 |
| Regulator page | bfarm.de |
At a glance
- No 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