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VENTANA HE 600 Eosin

Ventana Medical Systems, Inc. · Model 06544304001 · UDI-DI 04015630974757

HYB
10
510(k) clearances
0
Adverse events
3
Recalls
38
Facilities

Recalls

DateFirmReason
2010-01-06Wescor, IncStains used for diagnostic use may be contaminated with bacteria.
2010-01-06Wescor, IncStains used for diagnostic use may be contaminated with bacteria.
2010-01-06Wescor, IncStains used for diagnostic use may be contaminated with bacteria.

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Data 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.