Device recall
Z-1864-2017: Software version 4.44A utilized on the BD MAX System
FDA device recall · Class II · BD LIFE SCIENCES
Key facts
| Recall number (Z-number) | Z-1864-2017 |
|---|---|
| Recall event | 76900 |
| Product | Software version 4.44A utilized on the BD MAX System |
| Product code | NSX |
| Recalling firm | BD LIFE SCIENCES |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Apr 19, 2017 |
| 510(k) numbers | K111860 |
| FEI number | 3013091131 |
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