Device recall
Z-1912-2011: Penner Manufacturing Transfer Electric Cascade Patient Transfer/Lift System…
FDA device recall · Class II · Penner Mfg Inc
Key facts
| Recall number (Z-number) | Z-1912-2011 |
|---|---|
| Recall event | 56977 |
| Product | Penner Manufacturing Transfer Electric Cascade Patient Transfer/Lift System, Models 382000-1 (right entry) and 382000-1L (left entry). The firm name on the label is Penner Manufacturing Inc., Aurora, NE. For use with bathing systems in nursing homes, hospitals, and assisted living facilities to… |
| Product code | FNG |
| Recalling firm | Penner Mfg Inc |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Apr 8, 2011 |
| FEI number | 1922538 |
At a glance
- None Linked 510(k)s
- 10–99 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