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QBC Diagnostics
DRUCKER DIAGNOSTICS · Model 425740 · UDI-DI 00858092006031
10
510(k) clearances
30
Adverse events
4
Recalls
18
Facilities
Description
QBC Centrifuge - Capillary Tube Centrifuge
Recalls
| Date | Firm | Reason |
|---|---|---|
| 2009-11-21 | Hettich Instruments Management I | Centrifuge Rotor Failure: may crack, break, and explode outside the centrifuge. |
| 2009-11-21 | Hettich Instruments Management I | Centrifuge Rotor Failure: may crack, break, and explode outside the centrifuge. |
| 2009-11-21 | Hettich Instruments Management I | Centrifuge Rotor Failure: may crack, break, and explode outside the centrifuge. |
| 2009-11-21 | Hettich Instruments Management I | Centrifuge Rotor Failure: may crack, break, and explode outside the centrifuge. |
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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.