Device recall
Z-1869-2008: ON-Q PainBuster Infusion Pump (270 ml, 5 ml/hr), REF PS6504, Part No. 5001260…
FDA device recall · Class II · I-Flow Corporation
Key facts
| Recall number (Z-number) | Z-1869-2008 |
|---|---|
| Recall event | 48428 |
| Product | ON-Q PainBuster Infusion Pump (270 ml, 5 ml/hr), REF PS6504, Part No. 5001260. The pump is indicated for continuous and/or intermittent delivery of medication (such as local anesthetics or narcotics) to or around surgical wound sites and/or close proximity to nerves for preoperative, perioperative… |
| Product code | MEB |
| Recalling firm | I-Flow Corporation |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Feb 5, 2010 |
| 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