Device recall
Z-0835-2013: VACUETTE Safety Blood Collection Set + Luer Adapter, 23x12" Safety Blood Collect…
FDA device recall · Class II · Greiner Bio-One North America, Inc.
Key facts
| Recall number (Z-number) | Z-0835-2013 |
|---|---|
| Recall event | 64321 |
| Product | VACUETTE Safety Blood Collection Set + Luer Adapter, 23x12" Safety Blood Collect LA Product, Item number 450096. Usage: The Safety Blood Collection Set is used in routine venipuncture procedures. |
| Product code | FMI |
| Recalling firm | Greiner Bio-One North America, Inc. |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Oct 29, 2013 |
| 510(k) numbers | K011786 |
| 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