International safety notice
Kits y equipos de cateterismo epidural Arrow ®. Ver códigos de producto afectados en la nota de aviso de la empresa
Spain / AEMPS · ESP · Feb 24, 2020
Key facts
| Title | Kits y equipos de cateterismo epidural Arrow ®. Ver códigos de producto afectados en la nota de aviso de la empresa |
|---|---|
| Regulator | Spain / AEMPS |
| Country | ESP |
| Brand | Kits y equipos de cateterismo epidural Arrow ®. Ver códigos de producto afectados en la nota de aviso de la empresa |
| Manufacturer | Teleflex Medical, EE.UU. |
| Models | 71F19D2237, 13F19A0796, 918300462, 23F19G0305, 71F19E1144, 71F19D0826, 71F19E0149, MTO-05500-SU, 71F19A0623, 13F18J0481, 71F19G2837, 71F19C0748 and 492 more |
| Event type | Safety Notice |
| Date | Feb 24, 2020 |
At a glance
- No Recall
- Yes 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