Device recall
Z-2111-2009: I-Flow Corporation Easy Pump LT 60-24 (60 ml x 2 ml/hr), REF: 04434366…
FDA device recall · Class II · I-Flow Corporation
Key facts
| Recall number (Z-number) | Z-2111-2009 |
|---|---|
| Recall event | 50802 |
| Product | I-Flow Corporation Easy Pump LT 60-24 (60 ml x 2 ml/hr), REF: 04434366, assembled in Mexico. The Easypump LT is indicated for continuous and/or intermittent infusion of medication for general infusion use, including antibiotic delivery, chemotherapy and pain management. |
| Product code | MEB |
| Recalling firm | I-Flow Corporation |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Feb 4, 2010 |
| 510(k) numbers | K052117 |
| FEI number | 3011270181 |
At a glance
- 1–9 Linked 510(k)s
- 1–9 Products in the same recall event
- 100–999 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