International safety notice
IMMULITE/IMMULITE 1000 AlaTOP Allergy Screen, nº de catálogo LKAT e IMMULITE 2000/IMMULITE 2000 XPi AlaTOP Allergy Screen, nº de catálogo L2KAT2
Spain / AEMPS · ESP · Nov 11, 2021
Key facts
| Title | IMMULITE/IMMULITE 1000 AlaTOP Allergy Screen, nº de catálogo LKAT e IMMULITE 2000/IMMULITE 2000 XPi AlaTOP Allergy Screen, nº de catálogo L2KAT2 |
|---|---|
| Regulator | Spain / AEMPS |
| Country | ESP |
| Brand | IMMULITE/IMMULITE 1000 AlaTOP Allergy Screen, nº de catálogo LKAT e IMMULITE 2000/IMMULITE 2000 XPi AlaTOP Allergy Screen, nº de catálogo L2KAT2 |
| Manufacturer | Siemens Healthcare Inc, Reino Unido |
| Models | 91.822.52.89, 2021-535, 02032, LKAT1IMMULITE, 28906, 2105.A.OUS, 10380869, 21-05.B.OUS, 2021-611, LKAT1, 72525, 10380878 and 4 more |
| Event type | Safety Notice |
| Date | Nov 11, 2021 |
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