FDA Device recall Z-1523-2022
Power electronic box, Part #AS-0066, subassembly for the MyoCycle MC-2
- FDA Device
- Class II
- terminated
- Published 2022-08-24
On 2022-08-24 the FDA classified a Class II recall of Power electronic box, Part #AS-0066, subassembly for the MyoCycle MC-2 by Myolyn, citing screws mounting an internal power supply may come loose during shipping resulting in increased risk of high voltage electrical shock.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-1523-2022 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2022-07-19 |
| Published | 2022-08-24 |
| Last updated | 2026-09-13 11:56 UTC |
| Company | Myolyn |
| Distribution | AZ, CA, CT, FL, GA, ID, IL, KY, MA, MI, MN, MO, NC, NJ, NM, NY, OH, OR, TX, UT, VA, WA, WI |
Product
Power electronic box, Part #AS-0066, subassembly for the MyoCycle MC-2.
Reason
Screws mounting an internal power supply may come loose during shipping resulting in increased risk of high voltage electrical shock.
Identifiers
| code_info | Serial numbers 000800 thru 000819, 000821 thru 000822, 000824 thru 000827, 000829 thru 000831, 000835, 000836, 000840 t…Serial numbers 000800 thru 000819, 000821 thru 000822, 000824 thru 000827, 000829 thru 000831, 000835, 000836, 000840 thru 000842, 000850 thru 000852, and 000857 thru 000859; UDI 000861553000417 |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:56 UTC. Current status: terminated.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-1523-2022%22
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