Device recall
Z-0951-2017: Natus Warmette Blanket Cabinet and Warmette Dual Cabinet The Natus Warmette…
FDA device recall · Class II · Natus Manufacturing Limited
Key facts
| Recall number (Z-number) | Z-0951-2017 |
|---|---|
| Recall event | 75846 |
| Product | Natus Warmette Blanket Cabinet and Warmette Dual Cabinet The Natus Warmette Blanket Cabinet is designed to store and warm blankets and hospital linens; while, the Natus Warmette Dual Cabinet is designed to store and warm blankets and hospital linens in one compartment and fluids (irrigation and/or… |
| Product code | LGZ |
| Recalling firm | Natus Manufacturing Limited |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Jun 24, 2019 |
| 510(k) numbers | K132110 |
| FEI number | 3005581270 |
At a glance
- 1–9 Linked 510(k)s
- 1–9 Products in the same recall event
- 10–99 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