Device recall
Z-0086-06: Serum Blood Collection Tubes
FDA device recall · Class II · Greiner VACUETTE North America
Key facts
| Recall number (Z-number) | Z-0086-06 |
|---|---|
| Recall event | 32826 |
| Product | Serum Blood Collection Tubes |
| Product code | JKA |
| Recalling firm | Greiner VACUETTE North America |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Nov 16, 2005 |
| 510(k) numbers | K960858 |
| FEI number | 3001451379 |
At a glance
- 1–9 Linked 510(k)s
- 1–9 Products in the same recall event
- 100–999 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