Device recall
Z-0741-03: Easypump LT 60-24 Easypump Infusion Pump (60 ml x 2 ml/hr)
FDA device recall · Class II · I-Flow Corporation
Key facts
| Recall number (Z-number) | Z-0741-03 |
|---|---|
| Recall event | 25903 |
| Product | Easypump LT 60-24 Easypump Infusion Pump (60 ml x 2 ml/hr) |
| Recalling firm | I-Flow Corporation |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Nov 20, 2003 |
| 510(k) numbers | K991513 |
| FEI number | 3011270181 |
At a glance
- 1–9 Linked 510(k)s
- 1–9 Products in the same recall event
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