International safety notice
Kit Panocell®-10, Ficin-Treated Reagent Red Blood Cells Referencia: 0002385 UDI-DI: 10888234000310
Spain / AEMPS · ESP · Jul 9, 2024
Key facts
| Title | Kit Panocell®-10, Ficin-Treated Reagent Red Blood Cells Referencia: 0002385 UDI-DI: 10888234000310 |
|---|---|
| Regulator | Spain / AEMPS |
| Country | ESP |
| Brand | Kit Panocell®-10, Ficin-Treated Reagent Red Blood Cells Referencia: 0002385 UDI-DI: 10888234000310 |
| Manufacturer | Immucor, Inc. EEUU. |
| Models | 91.822.52.89, 855.466.8267, 21-23, 63303, 30071EE, LOTE19919-E, 107938, 0002385, 32692, INC.3130, FA-NOR-24-05, 113560056 and 14 more |
| Event type | Safety Notice |
| Date | Jul 9, 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