Home › Siemens Healthcare Diagnostics Inc. › ADVIA® 120/2120/2120i TESTpoint High Control
ADVIA® 120/2120/2120i TESTpoint High Control
Siemens Healthcare Diagnostics Inc. · Model 10312291 · UDI-DI 00630414224404
1
510(k) clearances
2
Adverse events
3
Recalls
9
Facilities
Description
ADVIA®120/2120/2120i TESTpoint™ High Control
Recalls
| Date | Firm | Reason |
|---|---|---|
| 2025-06-04 | Siemens Healthcare Diagnostics, Inc. | Products have the incorrect platelet (PLT) value assignments for the ADVIA 120/2120/2120i Hematology Systems. |
| 2025-06-04 | Siemens Healthcare Diagnostics, Inc. | Products have the incorrect platelet (PLT) value assignments for the ADVIA 120/2120/2120i Hematology Systems. |
| 2025-06-04 | Siemens Healthcare Diagnostics, Inc. | Products have the incorrect platelet (PLT) value assignments for the ADVIA 120/2120/2120i Hematology Systems. |
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Get your free API keyRead the docsData compiled from public U.S. FDA sources (GUDID, 510(k)/PMA, MAUDE, recalls, establishment registration). Adverse-event reports are unverified and do not establish causation. Informational only — not medical, clinical, or regulatory advice.