International safety notice
Corrective action for the Curved Reinforced Endotracheal Tubes and other devices for tracheal intubation, Teleflex Medical
Germany / BfArM · DEU · Dec 17, 2014
Key facts
| Title | Corrective action for the Curved Reinforced Endotracheal Tubes and other devices for tracheal intubation, Teleflex Medical |
|---|---|
| Regulator | Germany / BfArM |
| Country | DEU |
| Brand | tracheal intubation, Teleflex Medical |
| Manufacturer | Corrective action for the Curved Reinforced Endotracheal Tubes and other devices for tracheal intubation, Teleflex Medical |
| Models | 13IG01, 13IG32C, 12AG29, 11JG21, 13FG34C, 13IG31, 11KG39, 13EG02, 12DG12, 13AG17, 13LG34, 14HG03 and 760 more |
| Date | Dec 17, 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