Device recall
Z-2252-2009: Flexiflo Quantum Enteral Pump Model # 50596, 50598 and 59322. The Flexiflo…
FDA device recall · Class II · Abbott Nutrition, Abbott Laboratories
Key facts
| Recall number (Z-number) | Z-2252-2009 |
|---|---|
| Recall event | 53207 |
| Product | Flexiflo Quantum Enteral Pump Model # 50596, 50598 and 59322. The Flexiflo Quantum enteral pump is a medical device that is used to deliver enteral nutrition products to tube-fed patients. The pumps are generally used in hospitals, nursing homes, health care institutions and home care. |
| Product code | LZH |
| Recalling firm | Abbott Nutrition, Abbott Laboratories |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Sep 19, 2012 |
| 510(k) numbers | K913958 |
| 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