Device recall
Z-0090-2018: Reservoir Bag for WalkMed Infusion Pump Part Number 204820 Catalog Number…
FDA device recall · Class II · WalkMed, LLC
Key facts
| Recall number (Z-number) | Z-0090-2018 |
|---|---|
| Recall event | 78302 |
| Product | Reservoir Bag for WalkMed Infusion Pump Part Number 204820 Catalog Number IPR-86/10 65 mL and Reservoir Bag for WalkMed Infusion Pump Part Number 204821 Catalog Number IPR-150/10 150 mL The WalkMed Reservoir Bag is designed for use with the WalkMed 350VL Ambulatory pump and is intended to be used as… |
| Product code | FRN |
| Recalling firm | WalkMed, LLC |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Dec 27, 2017 |
| 510(k) numbers | K870524 |
| 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