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Tissue-Tek Film®
SAKURA FINETEK U.S.A., INC. · Model 4743 · UDI-DI 00615233078827
1
510(k) clearances
10
Adverse events
1
Recalls
13
Facilities
Description
Coverslipper with Barcode Reader
Recalls
| Date | Firm | Reason |
|---|---|---|
| 2018-09-04 | Leica Microsystems, Inc. | Product was assembled with an isolating fiberglass hose within the oven in the wrong position. This results in improper shielding from potential electrical shock. |
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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.