Myolyn Power Box Recall: High Voltage Shock Risk During Shipping

Take action

Contact the company & request your remedy

Recalling firmMyolyn Inc.6931 Nw 22nd St Ste A · Gainesville, FL 32653-1231

No email on file — write to the address above instead.

✎ GovInfoNow plain-language explainer

What happened, in plain English

Myolyn is recalling a power electronic box subassembly for the MyoCycle MC-2 because screws can become loose during shipping, increasing the risk of high voltage electrical shock. This could lead to serious injury if the device is used improperly.

Why it’s dangerous

Screws mounting the internal power supply can become loose during shipping. This may cause the power supply to malfunction, leading to high voltage electrical shock if the device is used.

Who’s affected

Owners of the MyoCycle MC-2 device with the specific serial numbers listed in the recall are affected. Users who have the power box subassembly with loose screws during shipping are at higher risk.

How to tell if you have this one

Check if your MyoCycle MC-2 has the power electronic box with serial numbers 000800-000819, 000821-000822, 000824-000827, 000829-000831, 000835-000836, 000840-000842, 000850-000852, or 000857-000859. The unique device identifier (UDI) 000861553000417 is also associated with this recall.

Brand
Myolyn
Category
Medical device

Based on the official FDA remedy

What to do — step by step

Check for Loose Screws
Inspect the power box subassembly for loose screws that could cause electrical shock during use.

✎ GovInfoNow

Questions people ask

What is the specific model of the device affected?

The MyoCycle MC-2 device with the Power electronic box subassembly (Part #AS-0066) is affected.

What serial numbers are affected?

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.

Is there a fix for this issue?

The recall does not specify a remedy, so no fix is provided in this notice.

Take action

Contact Myolyn

We’ve drafted a message you can send Myolyn to request your refund or repair — edit it as you like.

✉️ Open in email

Subject: Recall Z-1523-2022 — Myolyn Myolyn

Hello,

I own a Myolyn that is covered by recall Z-1523-2022 from Myolyn.

I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this?

Thank you.

Similar recalls

From people who’ve dealt with this

Experiences, tips, and questions from readers. Every comment is reviewed before it appears.

No comments yet — be the first to share your experience.

Where this comes from

The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.

Official source: FDA Recall #Z-1523-2022 (July 19, 2022) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for Z-1523-2022 to see it in context.
Plain-language summary written by qwen3:4b on August 19, 2026, from the official record above. Not reviewed by a person — if it conflicts with the FDA notice, the notice is correct. Report an error on this page.
GovInfoNow is an independent service and is not a government agency. We republish official FDA recall data; we don’t issue, amend or administer recalls.

Myolyn Inc. recalls Power electronic box, Part #AS-0066, subassembly for the MyoCycle MC-2.

Use caution until it’s fixed