Device recall
Z-0570-05: Flexiflo Quantum Enteral Pump
FDA device recall · Class II · Ross Products Division Abbott Laboratories
Key facts
| Recall number (Z-number) | Z-0570-05 |
|---|---|
| Recall event | 29856 |
| Product | Flexiflo Quantum Enteral Pump |
| Product code | LZH |
| Recalling firm | Ross Products Division Abbott Laboratories |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Apr 12, 2012 |
| 510(k) numbers | K944669 |
| FEI number | 1000136098 |
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