Device recall
Z-0551-04: Faaborg patient lift/hoist, battery operated lifts. The PL series lifts have…
FDA device recall · Class I · Moving Solutions, Inc.
Key facts
| Recall number (Z-number) | Z-0551-04 |
|---|---|
| Recall event | 28199 |
| Product | Faaborg patient lift/hoist, battery operated lifts. The PL series lifts have electric parallel base widening, with a weight capacity of 365 lbs. to 550 lbs. depending on the base model. Please note: the Faaborg Person Lift arm assembly can be interchanged on the various lift series bases. The arm… |
| Product code | FSA |
| Recalling firm | Moving Solutions, Inc. |
| Recall class | Class I |
| Status | Terminated |
| Termination date | Oct 22, 2007 |
| FEI number | 1000305914 |
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