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Liquichek
BIO-RAD LABORATORIES, INC. · Model 515 · UDI-DI 00847661003106
7
510(k) clearances
14
Adverse events
1
Recalls
13
Facilities
Description
Liquichek Sedimentation Rate Control Level 2 (A human whole blood assayed erythrocyte sedimentation rate control.)
Recalls
| Date | Firm | Reason |
|---|---|---|
| 2026-08-25 | POLYMEDCO, INC. / POLYMEDCO CANCER DIAGNOSTIC PRODUCTS, LLC | During use of an affected tube, the operator may encounter increased resistance when inserting the pipette. The resulting pressure buildup may cause the tube cap to detach or be fo |
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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.