Device recall
Z-0019-2015: ArjoHuntleigh Contoura C1000 series beds are designed to accommodate patients…
FDA device recall · Class II · Arjo Hospital Equipment AB
Key facts
| Recall number (Z-number) | Z-0019-2015 |
|---|---|
| Recall event | 67029 |
| Product | ArjoHuntleigh Contoura C1000 series beds are designed to accommodate patients weighing up to 990 lbs. (450 kg). Model C1000 is the basic bed. Model C1080 includes a weighing system and a power outlet for an ArjoHuntleigh approved mattress pump. Product Usage: The Contoura series bariatric beds are… |
| Product code | FNL |
| Recalling firm | Arjo Hospital Equipment AB |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Feb 14, 2018 |
| FEI number | 3002806395 |
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