Device recall
Z-0609-03: Compat DualFlo Enteral Delivery Pump Set with 1000-mL Twist Cap Formula Vinyl…
FDA device recall · Class II · Novartis Nutrition Corp
Key facts
| Recall number (Z-number) | Z-0609-03 |
|---|---|
| Recall event | 25470 |
| Product | Compat DualFlo Enteral Delivery Pump Set with 1000-mL Twist Cap Formula Vinyl Bag and 1000-mL Twist Cap Water Bag, Item number 19944700 |
| Product code | LZH |
| Recalling firm | Novartis Nutrition Corp |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Jun 24, 2004 |
| 510(k) numbers | K940555 |
| FEI number | 2110851 |
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