International safety notice
Recall for BD Venflon™ Pro Safety Peripheral IV Catheter, Becton Dickinson
Germany / BfArM · DEU · Jul 7, 2011
Key facts
| Title | Recall for BD Venflon™ Pro Safety Peripheral IV Catheter, Becton Dickinson |
|---|---|
| Regulator | Germany / BfArM |
| Country | DEU |
| Brand | BD Venflon™ Pro Safety Peripheral IV Catheter, Becton Dickinson |
| Manufacturer | Recall for BD Venflon™ Pro Safety Peripheral IV Catheter, Becton Dickinson |
| Models | 0355278, FA-11-045-104, 393227, 0333842, 0355277 |
| Date | Jul 7, 2011 |
| 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