Device recall
Z-1122-2014: Triton FP Infusion Pump, Part Number 400000, packaged in boxes. The Triton…
FDA device recall · Class II · WalkMed Infusion, LLC
Key facts
| Recall number (Z-number) | Z-1122-2014 |
|---|---|
| Recall event | 67545 |
| Product | Triton FP Infusion Pump, Part Number 400000, packaged in boxes. The Triton Volumetric Infusion Pump is indicated for delivering infusions of medications, as well as providing TPN (Total Parenteral Nutrition) and PCA (Patient Control Analgesia). It is intended for use in hospitals, ambulatory &… |
| Product code | FRN |
| Recalling firm | WalkMed Infusion, LLC |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Oct 6, 2014 |
| 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