Device recall
Z-2656-2014: Zenith Slide W-I-D-E Long Term Care Bed, Model(s) APS98674, APS9867406…
FDA device recall · Class II · GF Health Products, Inc./d.b.a.Basic American Metal Products
Key facts
| Recall number (Z-number) | Z-2656-2014 |
|---|---|
| Recall event | 69057 |
| Product | Zenith Slide W-I-D-E Long Term Care Bed, Model(s) APS98674, APS9867406, APS986741, APS986742, ZG58674, ZG78674, ZZ78674, ZZ98674, and ZZ98774. Designed for use within an institutional healthcare environment (i.e. assisted living, skilled nursing, transitional care, rehabilitation centers, etc.). |
| Product code | FNL |
| Recalling firm | GF Health Products, Inc./d.b.a.Basic American Metal Products |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Aug 11, 2015 |
| 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