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Henry Schein
HENRY SCHEIN, INC. · Model 1126910 · UDI-DI 00304040043370
10
510(k) clearances
30
Adverse events
4
Recalls
19
Facilities
Description
Centrifuge Micro-Hematocrit
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.