International safety notice
Cánula intravenosa BD Venflon Pro™. Ver números de catálogo afectados en el apéndice 1 de la nota de aviso de la empresa
Spain / AEMPS · ESP · May 28, 2021
Key facts
| Title | Cánula intravenosa BD Venflon Pro™. Ver números de catálogo afectados en el apéndice 1 de la nota de aviso de la empresa |
|---|---|
| Regulator | Spain / AEMPS |
| Country | ESP |
| Brand | Cánula intravenosa BD Venflon Pro™. Ver números de catálogo afectados en el apéndice 1 de la nota de aviso de la empresa |
| Manufacturer | Becton Dickinson Infusion Therapy AB, Suecia |
| Models | 0161046, 0112800, 9263978, 0304819, 0032455, 393210, 0066008, 0058199, 0157784, 9253437, 0007347, 0252810 and 122 more |
| Event type | Safety Notice |
| Date | May 28, 2021 |
At a glance
- No Recall
- Yes Field safety notice
- 1–9 Matching device models in FDA data
- 1–9 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