International safety notice
Corrective action for the product BRONCHIAL DOUBLE LUMEN TUBE SET, Teleflex Medical
Germany / BfArM · DEU · Dec 9, 2014
Key facts
| Title | Corrective action for the product BRONCHIAL DOUBLE LUMEN TUBE SET, Teleflex Medical |
|---|---|
| Regulator | Germany / BfArM |
| Country | DEU |
| Brand | the product BRONCHIAL DOUBLE LUMEN TUBE SET, Teleflex Medical |
| Manufacturer | Corrective action for the product BRONCHIAL DOUBLE LUMEN TUBE SET, Teleflex Medical |
| Models | 116100-000260, 115901-000080, 13IE36R, 13IT20, 14HT09, 14HT17, 116200-000350, 13JT11, 116200370, 14JT12, 14AT08, 14ET23 and 171 more |
| Date | Dec 9, 2014 |
| Regulator page | bfarm.de |
At a glance
- No Recall
- No Field safety notice
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