Device recall
Z-0615-2010: Haematokrit 20 Centrifuge with 2050 Rotor TYP #2014-01 and TYP#201424-01. Used…
FDA device recall · Class I · Hettich Instruments Management I
Key facts
| Recall number (Z-number) | Z-0615-2010 |
|---|---|
| Recall event | 53941 |
| Product | Haematokrit 20 Centrifuge with 2050 Rotor TYP #2014-01 and TYP#201424-01. Used for the purpose of determining the hematocrit count of a patient sample by way of applying centrifugal force in a manner that separates red blood cells and allows the proportion of red cell mass to plasma to be measured. |
| Product code | GKG |
| Recalling firm | Hettich Instruments Management I |
| Recall class | Class I |
| Status | Terminated |
| Termination date | Oct 25, 2011 |
| FEI number | 3004578971 |
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