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Tissue-Tek®
SAKURA FINETEK U.S.A., INC. · Model 4192 · UDI-DI 00615233078322
10
510(k) clearances
287
Adverse events
17
Recalls
113
Facilities
Description
Cassette Cabinet
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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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.