International safety notice
Recall for several products for inhalation therapy, Teleflex Medical
Germany / BfArM · DEU · Apr 29, 2014
Key facts
| Title | Recall for several products for inhalation therapy, Teleflex Medical |
|---|---|
| Regulator | Germany / BfArM |
| Country | DEU |
| Brand | inhalation therapy, Teleflex Medical |
| Manufacturer | Recall for several products for inhalation therapy, Teleflex Medical |
| Models | 026125, 101126, 40003628, 325127, 127126, 097127, 397127, 156126, 365127, 143127, 429127, 297127 and 569 more |
| Date | Apr 29, 2014 |
| Regulator page | bfarm.de |
At a glance
- No 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