International safety notice
Viales de hematíes reactivos Panoscreen I, II y III, referencia IMM0002381. UDI-DI: 10888234000303.
Spain / AEMPS · ESP · Jun 14, 2024
Key facts
| Title | Viales de hematíes reactivos Panoscreen I, II y III, referencia IMM0002381. UDI-DI: 10888234000303. |
|---|---|
| Regulator | Spain / AEMPS |
| Country | ESP |
| Brand | Viales de hematíes reactivos Panoscreen I, II y III, referencia IMM0002381. UDI-DI: 10888234000303. |
| Manufacturer | Immucor Inc., EEUU. |
| Models | 79382532, 04423610589, LOTE17845, 08908, FA-NOR-24-02, 107229, COBADEFF504, 32692, 2024-309, 855.466.8267, IMM0002381, 21-23 and 11 more |
| Event type | Safety Notice |
| Date | Jun 14, 2024 |
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