International safety notice
Risks when using the povidon-iodine containing MiniCap/OptiCap disconnect caps from Baxter
Germany / BfArM · DEU · Jan 13, 2006
Key facts
| Title | Risks when using the povidon-iodine containing MiniCap/OptiCap disconnect caps from Baxter |
|---|---|
| Regulator | Germany / BfArM |
| Country | DEU |
| Brand | Risks when using the povidon-iodine containing MiniCap/OptiCap disconnect caps from Baxter |
| Manufacturer | Risks when using the povidon-iodine containing MiniCap/OptiCap disconnect caps from Baxter |
| Models | 11576928, 1976170, 8648537, 8641223 |
| Date | Jan 13, 2006 |
| 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