Power electronic box — Class II medical device recall Z-1523-2022
Terminated recall by Myolyn Inc., reported 2022-08-24, distributed in AZ, CA, CT, FL, GA, ID, IL, KY…. Screws mounting an internal power supply may come loose during shipping resulting in increased risk of high vo
| Recall number | Z-1523-2022 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Myolyn Inc., Gainesville, FL, United States |
| Recall initiated | 2022-07-19 |
| Classified | 2022-08-16 |
| Reported by FDA | 2022-08-24 |
| Terminated | 2024-09-23 |
| Distributed | AZ, CA, CT, FL, GA, ID, IL, KY, MA, MI, MN, MO, NC, NJ, NM, NY, OH, OR, TX, UT, VA, WA, WI |
| Quantity | 45 devices |
| Serial numbers | 000800 |
| Model numbers | AS-0066 |
Product
Power electronic box, Part #AS-0066, subassembly for the MyoCycle MC-2.
Reason for recall
Screws mounting an internal power supply may come loose during shipping resulting in increased risk of high voltage electrical shock.
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-1523-2022. 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.