International safety notice
Corrective action for the Hudson RCI® SHERIDAN SHER-I-BRONCH® Endobronchial Tube, Teleflex Medical
Germany / BfArM · DEU · Jul 9, 2015
Key facts
| Title | Corrective action for the Hudson RCI® SHERIDAN SHER-I-BRONCH® Endobronchial Tube, Teleflex Medical |
|---|---|
| Regulator | Germany / BfArM |
| Country | DEU |
| Brand | the Hudson RCI® SHERIDAN SHER-I-BRONCH® Endobronchial Tube, Teleflex Medical |
| Manufacturer | Corrective action for the Hudson RCI® SHERIDAN SHER-I-BRONCH® Endobronchial Tube, Teleflex Medical |
| Models | 01A1400432, 73B1500354, 01J1300471, 01A1400576, 73L1400098, 5-16141, 73E1400114, 73H1400442, 01B1400242, 01A1400226, 01A1400436, 01B1400356 and 237 more |
| Date | Jul 9, 2015 |
| 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