Device recall
Z-1306-2015: Penner Patient Stretcher/Transfer Lift System Models 391000-1 and 392000-1 The…
FDA device recall · Class II · Penner Mfg Inc
Key facts
| Recall number (Z-number) | Z-1306-2015 |
|---|---|
| Recall event | 70151 |
| Product | Penner Patient Stretcher/Transfer Lift System Models 391000-1 and 392000-1 The Pacific Stretcher/Transfer Lift is used with Whirlpool or Aqua-Aire (air bubbling) bathing system intended for use in nursing homes, hospitals, and assisted living facilities to transfer and/or lift patients under the… |
| Product code | MMP |
| Recalling firm | Penner Mfg Inc |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Mar 10, 2016 |
| 510(k) numbers | K962288 |
| FEI number | 1922538 |
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