International safety notice
Recall for the Venous Bubble Trap VBT 160 and Custom Tubing Sets containing the Venous Bubble Trap VBT 160, Maquet Cardiopulmonary AG
Germany / BfArM · DEU · Aug 14, 2014
Key facts
| Title | Recall for the Venous Bubble Trap VBT 160 and Custom Tubing Sets containing the Venous Bubble Trap VBT 160, Maquet Cardiopulmonary AG |
|---|---|
| Regulator | Germany / BfArM |
| Country | DEU |
| Brand | the Venous Bubble Trap VBT 160 and Custom Tubing Sets containing the Venous Bubble Trap VBT 160, Maquet Cardiopulmonary AG |
| Manufacturer | Recall for the Venous Bubble Trap VBT 160 and Custom Tubing Sets containing the Venous Bubble Trap VBT 160, Maquet Cardiopulmonary AG |
| Models | 2014-08-06, PAGE3, PAGE2, 76437 |
| Date | Aug 14, 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