Device recall
Z-2305-2008: Flexiflo Quantum Pump Set with Piercing Pin and Flush Bag The product is used…
FDA device recall · Class II · Abbott Laboratories
Key facts
| Recall number (Z-number) | Z-2305-2008 |
|---|---|
| Recall event | 48725 |
| Product | Flexiflo Quantum Pump Set with Piercing Pin and Flush Bag The product is used with Quantum pump to deliver ready-to-hang (RTH) product in enterally-fed patients. |
| Product code | LZH |
| Recalling firm | Abbott Laboratories |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Sep 19, 2012 |
| 510(k) numbers | K915735 |
| FEI number | 1513768 |
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