Device recall
Z-1837-2013: Omnicycle Elite; US Importer and Distributor: Accelerated Care Plus, Reno NV…
FDA device recall · Class II · Accelerated Care Plus Corporation
Key facts
| Recall number (Z-number) | Z-1837-2013 |
|---|---|
| Recall event | 65498 |
| Product | Omnicycle Elite; US Importer and Distributor: Accelerated Care Plus, Reno NV. Manufactured by Medica Medizintechnik GmbH, Hochdorf, Germany. The product is indicated for powered exercise equipment intended for medical purposes. |
| Product code | BXB |
| Recalling firm | Accelerated Care Plus Corporation |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Oct 23, 2013 |
| FEI number | 1000119345 |
At a glance
- None Linked 510(k)s
- 1–9 Products in the same recall event
- 1–9 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