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Liquichek
BIO-RAD LABORATORIES, INC. · Model 172X · UDI-DI 00847661002192
1
510(k) clearances
2
Adverse events
2
Recalls
17
Facilities
Description
Liquichek Diabetes Control Level Trilevel MiniPak (A human whole blood assayed diabetes control.)
Recalls
| Date | Firm | Reason |
|---|---|---|
| 2018-10-18 | EUROTROL INC | Incorrect measurement results caused by microbial contamination of the product, results in values lower than assigned values |
| 2018-10-18 | EUROTROL INC | Incorrect measurement results caused by microbial contamination of the product, results in values lower than assigned values |
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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.