Device recall
Z-1405-2017: A-series lift - A625 Manual w/Load Cell & Wi-Fi, Omni Part No. 324124. Prism…
FDA device recall · Class II · ErgoSafe Products, LLC (DBA) Prism Medical
Key facts
| Recall number (Z-number) | Z-1405-2017 |
|---|---|
| Recall event | 76351 |
| Product | A-series lift - A625 Manual w/Load Cell & Wi-Fi, Omni Part No. 324124. Prism Medical. |
| Product code | FSA |
| Recalling firm | ErgoSafe Products, LLC (DBA) Prism Medical |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Dec 4, 2017 |
| FEI number | 3007802293 |
At a glance
- None Linked 510(k)s
- 1–9 Products in the same recall event
- 100–999 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