Device recall
Z-0750-2010: BD Q-Syte, Luer Access Split-Septum, 0.10 ml, REF 385100, Becton Dickinson…
FDA device recall · Class I · Becton Dickinson Medical Systems
Key facts
| Recall number (Z-number) | Z-0750-2010 |
|---|---|
| Recall event | 53749 |
| Product | BD Q-Syte, Luer Access Split-Septum, 0.10 ml, REF 385100, Becton Dickinson Infusion Therapy Systems Inc. |
| Product code | FPA |
| Recalling firm | Becton Dickinson Medical Systems |
| Recall class | Class I |
| Status | Terminated |
| Termination date | Oct 19, 2010 |
| 510(k) numbers | K013621 |
| FEI number | 1710034 |
At a glance
- 1–9 Linked 510(k)s
- 10–99 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