Device recall
Z-0211-2009: Separation Technology ClearCRIT Capillary Tubes 75mm/1.1mm ID. Catalog number…
FDA device recall · Class II · Drummond Scientific Co
Key facts
| Recall number (Z-number) | Z-0211-2009 |
|---|---|
| Recall event | 49092 |
| Product | Separation Technology ClearCRIT Capillary Tubes 75mm/1.1mm ID. Catalog number 270-106. Separation Technology Inc, 1096 Rainer Drive, Altamonte Springs, FL 32714. Heparin-treated capillary tube used for spun hematocrit packed cell volume (PCV) determination. |
| Product code | GIO |
| Recalling firm | Drummond Scientific Co |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Dec 18, 2008 |
| FEI number | 2518153 |
At a glance
- None Linked 510(k)s
- 1–9 Products in the same recall event
- 10–99 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