Device recall
Z-1211-2023: Sprint 200 wheeled stretcher, Item numbers 1ES200-7, 1ES210-1, and 1ES211-1.
FDA device recall · Class II · Linet Spol. S.r.o.
Key facts
| Recall number (Z-number) | Z-1211-2023 |
|---|---|
| Recall event | 91492 |
| Product | Sprint 200 wheeled stretcher, Item numbers 1ES200-7, 1ES210-1, and 1ES211-1. |
| Product code | FPO |
| Recalling firm | Linet Spol. S.r.o. |
| Recall class | Class II |
| Status | Open, Classified |
| FEI number | 3008058231 |
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