Home › BIO-RAD LABORATORIES, INC. › Liquichek
Liquichek
BIO-RAD LABORATORIES, INC. · Model 760 · UDI-DI 00847661002963
1
510(k) clearances
2
Adverse events
3
Recalls
9
Facilities
Description
Liquichek Hematology-16 Control Trilevel (A human whole blood assayed hematology 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. |
Query this across every FDA database — by API.
Linked GUDID · 510(k)/PMA · MAUDE · recalls · establishments. Free tier, no card required.
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.