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Fresh Cells

DIAGNOSTIC HYBRIDS, INC. · Model 84-T025 · UDI-DI 30014613334262

KIR Prescription
10
510(k) clearances
1
Adverse events
1
Recalls
7
Facilities

Description

VERO FLASK 25 SQ CM

Recalls

DateFirmReason
2009-01-21Diagnostic Hybrids IncDuring QC post release monitoring, the firm determined that the monolayer culture of rabbit kidney cells previously distributed by the firm, appeared to contain another type of cel

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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.