Device recall
Z-0732-2017: Lumex, Patriot Full Electric Homecare Bed, & Patriot LX Full Electric Homecare…
FDA device recall · Class II · GF Health Products, Inc
Key facts
| Recall number (Z-number) | Z-0732-2017 |
|---|---|
| Recall event | 75460 |
| Product | Lumex, Patriot Full Electric Homecare Bed, & Patriot LX Full Electric Homecare Bed containing the Okin Dumat 3 Head/Foot Motors. Description Part Number Motor and Pendant Patriot Full Electric 120V 690-3001-943 / 690-7001-943 Boxed Full Electric 220V Motor 690-3220-943 Motor and Pendant Patriot LX… |
| Product code | FNL |
| Recalling firm | GF Health Products, Inc |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Apr 29, 2019 |
| FEI number | 2183191 |
At a glance
- None 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