Device recall
Z-0014-2018: Carina Mobile Lifts, Models: a) Carina350EM, REF 6060011 b) Carina350EML, REF…
FDA device recall · Class II · Handicare AB
Key facts
| Recall number (Z-number) | Z-0014-2018 |
|---|---|
| Recall event | 78130 |
| Product | Carina Mobile Lifts, Models: a) Carina350EM, REF 6060011 b) Carina350EML, REF 60600012 c) Carina350EE, REF 60600009 |
| Product code | FSA |
| Recalling firm | Handicare AB |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Dec 17, 2018 |
| FEI number | 3009481053 |
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