Omnicycle Elite — Class II medical device recall Z-1837-2013
Terminated recall by Accelerated Care Plus Corporation, reported 2013-08-07, distributed nationwide. An anomaly in the firmware that may cause Omnicycle Elite to operate at a speed other than what was previously
| Recall number | Z-1837-2013 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Accelerated Care Plus Corporation, Reno, NV, United States |
| Recall initiated | 2013-06-12 |
| Classified | 2013-07-31 |
| Reported by FDA | 2013-08-07 |
| Terminated | 2013-10-23 |
| Distributed | Nationwide (US) |
| Quantity | 1,001 units |
| Reason classes | software |
| Serial numbers | 1034-000-00-09033104, 1034-000-00-09033107, 1034-000-00-09033108, 1034-000-00-09033119, 1034-000-00-09033120, 1034-000-00-09033121, 1034-000-00-09033122, 1034-000-00-09033132, 1034-000-01-09073002, 1034-000-01-09073005, 1034-000-01-09073018, 1034-000-01-09073021, 1034-000-01-09073030, 1034-000-01-09073123, 1034-000-01-09073129, 1034-000-01-09073130, 1034-000-01-09073134, 1034-000-01-09073136, 1034-000-01-09073142, 1034-000-01-09073146, 1034-000-01-09073147, 1034-000-01-09090034, 1034-000-01-09101119, 1034-000-01-09101126, 1034-000-01-09101127 and 475 more |
| Model numbers | A000-533 |
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.
Reason for recall
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.
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/Z-1837-2013. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.