Device recall
Z-0307-2011: WalkMed Triton Pole Mount Infusion Pump, Catalog 300000. Indicated for…
FDA device recall · Class I · Walkmed Infusion LLC
Key facts
| Recall number (Z-number) | Z-0307-2011 |
|---|---|
| Recall event | 56750 |
| Product | WalkMed Triton Pole Mount Infusion Pump, Catalog 300000. Indicated for delivering infusions of medications, as well as providing total parenteral nutrition, and patient controlled analgesia. |
| Product code | FRN |
| Recalling firm | Walkmed Infusion LLC |
| Recall class | Class I |
| Status | Terminated |
| Termination date | Mar 14, 2012 |
| 510(k) numbers | K070529 |
| FEI number | 3000204189 |
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