Device recall
Z-0568-2010: Paramed Polypropylene evacuation sled for non-ambulatory patients. Hand-carried…
FDA device recall · Class II · Paramed Systems
Key facts
| Recall number (Z-number) | Z-0568-2010 |
|---|---|
| Recall event | 53339 |
| Product | Paramed Polypropylene evacuation sled for non-ambulatory patients. Hand-carried stretcher. Product 11-778-01. |
| Product code | FPP |
| Recalling firm | Paramed Systems |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Jan 28, 2010 |
| FEI number | 3004828791 |
At a glance
- None 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