Device recall
Z-0242-2016: Triton Infusion Pump (model 300000) and Triton fp Infusion Pump (model 400000)…
FDA device recall · Class II · WalkMed Infusion, LLC
Key facts
| Recall number (Z-number) | Z-0242-2016 |
|---|---|
| Recall event | 72331 |
| Product | Triton Infusion Pump (model 300000) and Triton fp Infusion Pump (model 400000) (proprietary name: AFF (Mark I) Volumetric Infusion Pump). Used to pump fluids into a patient in a controlled manner. |
| Product code | FRN |
| Recalling firm | WalkMed Infusion, LLC |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Jul 12, 2016 |
| 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