Device recall
Z-2860-2011: I-Flow ON-Q with Select-A-Flow Pumps, Intended for continuous and/or…
FDA device recall · Class II · I-Flow Corporation
Key facts
| Recall number (Z-number) | Z-2860-2011 |
|---|---|
| Recall event | 59148 |
| Product | I-Flow ON-Q with Select-A-Flow Pumps, Intended for continuous and/or intermittent delivery of medication to and around surgical wound sites and/or close proximity to nerves for preoperative, perioperative and postoperative regional anesthesia and pain management. It is a controller that allows the… |
| Product code | MEB |
| Recalling firm | I-Flow Corporation |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Aug 9, 2012 |
| 510(k) numbers | K063530 |
| 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