Device recall
Z-1367-2013: SLIDERPREP PLUS SLIDE PREPARATION CENTRIFUGE. Produce a monolayer of cells onto…
FDA device recall · Class II · Separation Technology, Inc.
Key facts
| Recall number (Z-number) | Z-1367-2013 |
|---|---|
| Recall event | 64718 |
| Product | SLIDERPREP PLUS SLIDE PREPARATION CENTRIFUGE. Produce a monolayer of cells onto a glass slide from any fluid suspension. |
| Product code | IFB |
| Recalling firm | Separation Technology, Inc. |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Dec 24, 2013 |
| FEI number | 1721649 |
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