Device recall
Z-0931-2020: PediaLift Access Device, Device Identifier: B751PDLFT0
FDA device recall · Class II · PediaLift LLC
Key facts
| Recall number (Z-number) | Z-0931-2020 |
|---|---|
| Recall event | 84591 |
| Product | PediaLift Access Device, Device Identifier: B751PDLFT0 |
| Product code | FMS |
| Recalling firm | PediaLift LLC |
| Recall class | Class II |
| Status | Terminated |
| Termination date | May 15, 2020 |
| FEI number | 3012103974 |
At a glance
- None Linked 510(k)s
- 1–9 Products in the same recall event
- 1–9 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