International safety notice
Reactivo Anti-Lea (Anti-LE1) BioClone® 2.0. Ref. 6901859; UDI: 10758750007271
Spain / AEMPS · ESP · Jul 13, 2022
Key facts
| Title | Reactivo Anti-Lea (Anti-LE1) BioClone® 2.0. Ref. 6901859; UDI: 10758750007271 |
|---|---|
| Regulator | Spain / AEMPS |
| Country | ESP |
| Brand | Reactivo Anti-Lea (Anti-LE1) BioClone® 2.0. Ref. 6901859; UDI: 10758750007271 |
| Manufacturer | Ortho Clinical Diagnostics Inc. EE UU. |
| Models | LAB170AX, LAB168AX, 10758750007271, 23-JUL-2023, 6901859, 10-SEP-2023, ANTI-LE1, CL2022-164A_EU, 28022, 14-MAY-2023, LAB169AX, 81798 and 5 more |
| Event type | Safety Notice |
| Date | Jul 13, 2022 |
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