Device recall
Z-1075-2010: Medical Action Industries, Dialysis Kit, using BD Q-Syte Luer Access Split…
FDA device recall · Class I · Medical Action Industries Inc
Key facts
| Recall number (Z-number) | Z-1075-2010 |
|---|---|
| Recall event | 53880 |
| Product | Medical Action Industries, Dialysis Kit, using BD Q-Syte Luer Access Split Septum (BD #385100), Part number: 57977. |
| Product code | FPA |
| Recalling firm | Medical Action Industries Inc |
| Recall class | Class I |
| Status | Terminated |
| Termination date | Jun 1, 2011 |
| 510(k) numbers | K013621 |
| FEI number | 1030451 |
At a glance
- 1–9 Linked 510(k)s
- 1–9 Products in the same recall event
- 1,000+ 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