Device recall
Z-2219-2016: The pump (with cushioning foam inserts) is packaged in a single pump box. Four…
FDA device recall · Class II · WalkMed Infusion, LLC
Key facts
| Recall number (Z-number) | Z-2219-2016 |
|---|---|
| Recall event | 74436 |
| Product | The pump (with cushioning foam inserts) is packaged in a single pump box. Four pump boxes are placed in an over-shipper for distribution. |
| Product code | FRN |
| Recalling firm | WalkMed Infusion, LLC |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Apr 28, 2017 |
| 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