International safety notice
Recall for VaxcelTM Port and VaxcelTM Port with PASVTM Valve, Navilyst Medical Inc.
Germany / BfArM · DEU · Aug 17, 2010
Key facts
| Title | Recall for VaxcelTM Port and VaxcelTM Port with PASVTM Valve, Navilyst Medical Inc. |
|---|---|
| Regulator | Germany / BfArM |
| Country | DEU |
| Brand | VaxcelTM Port and VaxcelTM Port with PASVTM Valve, Navilyst Medical Inc. |
| Manufacturer | Recall for VaxcelTM Port and VaxcelTM Port with PASVTM Valve, Navilyst Medical Inc. |
| Models | 1305978, 1381887, 1373685, 1346939, 1307354, 1239323, 1307625, 1290364, 1380992, 1373686, 1292669, 1229804 and 512 more |
| Date | Aug 17, 2010 |
| Regulator page | bfarm.de |
At a glance
- No Recall
- No Field safety notice
- 10–99 Matching device models in FDA data
- 10–99 Matching catalog numbers 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