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Cyto-Tek®

SAKURA FINETEK U.S.A., INC. · Model 4310 · UDI-DI 00615233078438

KDT

510(k) clearances

287

Adverse events

Recalls

113

Facilities

Description

Mailer

Recalls

Date	Firm	Reason
2011-01-09	Heritage Labs International LLC	Kits contain recalled Triad alcohol pads
2011-01-09	Heritage Labs International LLC	Kits contain recalled Triad alcohol pads
2011-01-09	Heritage Labs International LLC	Kits contain recalled Triad alcohol pads
2011-01-09	Heritage Labs International LLC	Kits contain recalled Triad alcohol pads
2011-01-09	Heritage Labs International LLC	Kits contain recalled Triad alcohol pads
2011-01-09	Heritage Labs International LLC	Kits contain recalled Triad alcohol pads
2011-01-09	Heritage Labs International LLC	Kits contain recalled Triad alcohol pads
2011-01-09	Heritage Labs International LLC	Kits contain recalled Triad alcohol pads
2011-01-09	Heritage Labs International LLC	Kits contain recalled Triad alcohol pads
2011-01-09	Heritage Labs International LLC	Kits contain recalled Triad alcohol pads

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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.