Drug recall
Lumex, Patriot Full Electric Homecare Bed, & Patriot LX Full Electric Homecare Bed containing the Okin Dumat 3…
FDA recall event 75460 · Class II · GF Health Products, Inc
Key facts
| Event ID | 75460 |
|---|---|
| Recall numbers | Z-0732-2017 |
| Recalling firm | GF Health Products, Inc |
| Product type | Devices |
| Products | 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… |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Firm Initiated |
| Reason for recall | GF Health Products, Inc., in conjunction with OKIN America, has initiated a voluntary field correction affecting the OKIN America "DUOMAT 3" Head/Foot motor used in the manufacture of our Lumex… |
| Initiation date | Sep 30, 2016 |
| Report date | Dec 21, 2016 |
| Termination date | Apr 29, 2019 |
| City | Fond Du Lac |
| State | WI |
| Country | United States |
| FEI number | 2183191 |
At a glance
- 1–9 Products in this recall
- 1–9 FDA inspections of this firm (FEI)
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About FDA drug and product recalls
FDA enforcement reports list recalls of drugs, biologics, foods and other FDA-regulated products, classified by the potential health hazard.
Source: U.S. Food and Drug Administration (FDA), Enforcement Reports · Source date: