Device recall
Z-0728-2017: Carry bar which is an accessory to a lift used for patients in hospitals and…
FDA device recall · Class II · ErgoSafe Products, LLC (DBA) Prism Medical
Key facts
| Recall number (Z-number) | Z-0728-2017 |
|---|---|
| Recall event | 74488 |
| Product | Carry bar which is an accessory to a lift used for patients in hospitals and other facilities. Recall impacts the following model numbers: 360741, 360750, 360751, 360755, 360755 Rev B, 360756, and 360757. |
| Product code | FSA |
| Recalling firm | ErgoSafe Products, LLC (DBA) Prism Medical |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Jul 18, 2018 |
| 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