International safety notice
Corrective action for Floseal Hemostatic Matrix (Floseal VH S/D), Baxter Healthcare
Germany / BfArM · DEU · Oct 13, 2014
Key facts
| Title | Corrective action for Floseal Hemostatic Matrix (Floseal VH S/D), Baxter Healthcare |
|---|---|
| Regulator | Germany / BfArM |
| Country | DEU |
| Brand | Floseal Hemostatic Matrix (Floseal VH S/D), Baxter Healthcare |
| Manufacturer | Corrective action for Floseal Hemostatic Matrix (Floseal VH S/D), Baxter Healthcare |
| Models | VNY1N022, VNY1N015, VNY1N003, VNY1N014, VNY1N018, VNY2P002, VNY1N001, VNY2P004, VNY1N012, VNY1N023, VNY1N007, VNY1N025 and 20 more |
| Date | Oct 13, 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