Home › SAKURA FINETEK U.S.A., INC. › Tissue-Tek® Glas™
Tissue-Tek® Glas™
SAKURA FINETEK U.S.A., INC. · Model 6419 · UDI-DI 00615233080653
1
510(k) clearances
10
Adverse events
1
Recalls
12
Facilities
Description
Mounting Medium; 1 x 16 oz
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. |
Query this across every FDA database — by API.
Linked GUDID · 510(k)/PMA · MAUDE · recalls · establishments. Free tier, no card required.
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.
