International safety notice
Recall for the Thoracic Vent Procedure Tray, Uresil, LLC
Germany / BfArM · DEU · Jul 13, 2015
Key facts
| Title | Recall for the Thoracic Vent Procedure Tray, Uresil, LLC |
|---|---|
| Regulator | Germany / BfArM |
| Country | DEU |
| Brand | the Thoracic Vent Procedure Tray, Uresil, LLC |
| Manufacturer | Recall for the Thoracic Vent Procedure Tray, Uresil, LLC |
| Models | 2015-02-25, 4L136, 4L135, 4J901, 60077, 847.982.0106, 847-982-0106, 4J870, 4H809R, 4H789R, TV11-10, 4J831R and 11 more |
| Date | Jul 13, 2015 |
| Regulator page | bfarm.de |
At a glance
- No Recall
- No Field safety notice
- 1–9 Matching device models 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