Device recall
Z-1748-2014: Tissue-Tek PARAFORM PROC/EMB/MEDIUM, FORMULA 3 - 8x1Kg. for diagnostic chemistry…
FDA device recall · Class II · Sakura Finetek USA Inc
Key facts
| Recall number (Z-number) | Z-1748-2014 |
|---|---|
| Recall event | 68081 |
| Product | Tissue-Tek PARAFORM PROC/EMB/MEDIUM, FORMULA 3 - 8x1Kg. for diagnostic chemistry use. Sakura Finetek USA, Inc. |
| Product code | KEO |
| Recalling firm | Sakura Finetek USA Inc |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Sep 2, 2014 |
| FEI number | 2083544 |
At a glance
- None Linked 510(k)s
- 1–9 Products in the same recall event
- 1–9 Recalled products with this product code
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About FDA device recalls (products)
Each recalled device product receives a Z-number. Recall details such as root cause, distribution and firm actions are available in Orca1.
Source: U.S. Food and Drug Administration (FDA), Medical Device Recalls database