International safety notice
Urgent Field Safety Notice for ADVIA 2120/2120i Hematology System by Siemens Healthcare Diagnostics Inc. Tarrytown
Germany / BfArM · DEU · May 13, 2022
Key facts
| Title | Urgent Field Safety Notice for ADVIA 2120/2120i Hematology System by Siemens Healthcare Diagnostics Inc. Tarrytown |
|---|---|
| Regulator | Germany / BfArM |
| Country | DEU |
| Brand | ADVIA 2120/2120i Hematology System |
| Manufacturer | Siemens Healthcare Diagnostics Inc. Tarrytown |
| Models | 11314044, 10488923, 11219529, 10374454, 10285573, HSW21-01.B.OUS, 6.10.9, 10316162, 6.11.7, 10374453, 2120I, HSW2101.A.OUS and 6 more |
| Date | May 13, 2022 |
| Regulator page | bfarm.de |
At a glance
- No Recall
- No Field safety notice
- 10–99 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