Device recall
Z-2600-2021: LikoStretch 1900 Model Number: 3156051 - The combination of this products allows…
FDA device recall · Class II · Hill-Rom, Inc.
Key facts
| Recall number (Z-number) | Z-2600-2021 |
|---|---|
| Recall event | 88548 |
| Product | LikoStretch 1900 Model Number: 3156051 - The combination of this products allows the user to easily adjust/control the center of gravity during lift of patient. |
| Product code | FSA |
| Recalling firm | Hill-Rom, Inc. |
| Recall class | Class II |
| Status | Open, Classified |
| FEI number | 1824206 |
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