Device recall
Z-2157-2021: Zippie Voyage, early intervention stroller - Product Usage: is manually operated…
FDA device recall · Class II · Sunrise Medical (US) LLC
Key facts
| Recall number (Z-number) | Z-2157-2021 |
|---|---|
| Recall event | 88257 |
| Product | Zippie Voyage, early intervention stroller - Product Usage: is manually operated by a caregiver for purposes of assisting a disabled person while providing supportive elements for assisted transportation and seating for a child or small adult not to exceed 75 pounds. |
| Product code | INM |
| Recalling firm | Sunrise Medical (US) LLC |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Mar 28, 2025 |
| FEI number | 2937137 |
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