International safety notice
- Kits y conjuntos de cateterismo de la arteria radial Arrow® QuickFlash®. - Kit de cateterismo de la arteria/línea arterial radial Arrow® QuickFlash®. Ver códigos de producto y UDIs afectados en la nota de aviso de la empresa.
Spain / AEMPS · ESP · Feb 21, 2024
Key facts
| Title | - Kits y conjuntos de cateterismo de la arteria radial Arrow® QuickFlash®. - Kit de cateterismo de la arteria/línea arterial radial Arrow® QuickFlash®. Ver códigos de producto y UDIs afectados en la nota de aviso de la empresa. |
|---|---|
| Regulator | Spain / AEMPS |
| Country | ESP |
| Brand | - Kits y conjuntos de cateterismo de la arteria radial Arrow® QuickFlash®. - Kit de cateterismo de la arteria/línea arterial radial Arrow® QuickFlash®. Ver códigos de producto y UDIs afectados en la nota de aviso de la empresa. |
| Manufacturer | Arrow International LLC, EEUU. |
| Models | ASK-04220-FMH1, 14F23J0138, 14F22F0210, 14F22E0215, 33F23J0607, ASK-04500-HF-S, 14F22K0183, 14F22C0022, 33F23H0320, 240831, 14F22D0110, 13F22L0105 and 220 more |
| Event type | Safety Notice |
| Date | Feb 21, 2024 |
At a glance
- No Recall
- Yes 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