Device recall
Z-1389-2012: Pharmacy compounding system. It is a twenty-four source compounder for…
FDA device recall · Class II · Baxa Corporation
Key facts
| Recall number (Z-number) | Z-1389-2012 |
|---|---|
| Recall event | 52024 |
| Product | Pharmacy compounding system . It is a twenty-four source compounder for multi-source fluid mixing of both macro and micro ingredient down to 0.2 ml quantities. Product Usage: Pharmacy compounding System for parenteral macro and micro ingredients |
| Product code | NEP |
| Recalling firm | Baxa Corporation |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Apr 10, 2012 |
| FEI number | 1419106 |
At a glance
- None 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