Class II — Accelerated Care Plus Corporation
| Recalling firm | Accelerated Care Plus |
|---|---|
| Registered facility | ACCELERATED CARE PLUS CORP. (the firm's only registered facility) |
| Classification | Class II |
| Status | Terminated |
| Reason | An anomaly in the firmware that may cause Omnicycle Elite to operate at a speed other than what was previously set when in reverse mode. |
| 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. |
| Quantity | 1001 units |
| Distribution | Nationwide Distribution. |
| Initiated | 2013-06-12 |
| Classified | 2013-07-31 |
| Terminated | 2013-10-23 |
| Recall number | Z-1837-2013 |
| Initiation | Voluntary: Firm initiated |
Source: U.S. FDA via openFDA (opens in a new tab) (device registration & enforcement). Data as of 2026-10-06. Verify this recall record at FDA → (opens in a new tab)
Cite this record
RegWarden. “Class II recall — Accelerated Care Plus Corporation (Z-1837-2013).” Compiled from U.S. FDA public records (openFDA; FDA Data Dashboard). Data as of 2026-10-06. https://regwarden.com/recall/65498/
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