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.
FDA Recall Z-1837-2013 · Posted 2013-07-31
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Recalling FirmAccelerated Care Plus Corporation
Recall StatusTerminated
Product CodeBXB
Date Initiated2013-06-12
Date Terminated2013-10-23
Product Quantity1001 units
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.
Firm Action
Letters were issued on June 12, 2013 that included a memory stick with self loading software so consumers can update the device. Letters were sent by trackable method. Customers with questions or concerns should call Customer Support at 800-350-1100.
Root Cause
Software design
Distribution Pattern
Nationwide Distribution.
Official Source
View FDA Recall →Source: FDA Enforcement Report / Recall database. Always confirm against the official FDA record.
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