Device recall
Z-2263-2016: Dual Chamber Container fill with gravity/attached transfer sets, 250 mL / 1250…
FDA device recall · Class II · The Metrix Company
Key facts
| Recall number (Z-number) | Z-2263-2016 |
|---|---|
| Recall event | 74043 |
| Product | Dual Chamber Container fill with gravity/attached transfer sets, 250 mL / 1250 mL, 300 mL / 1700 mL, 500 mL / 2500 mL, 500 mL / 3500 mL |
| Product code | NEP |
| Recalling firm | The Metrix Company |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Apr 11, 2023 |
| 510(k) numbers | K960581 |
| FEI number | 1000117446 |
At a glance
- 1–9 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