Stop using now Medical device recall · FDA · Published November 28, 2023

mo-Vis Scoot Control Recall: Throttle Stuck Hazard

mo-Vis recalls Scoot Control R-net units due to throttle lever sticking, which may cause unwanted wheelchair movement and injury.

Plain-English summary generated from official FDA data by GovInfoNow · Published by Carlos Caban · How we make summaries

🇺🇸 FDA recall #Z-0713-2024Medical device mo-Vis ›

Stop using this now

In rare cases, the lever of the throttle can get temporarily stuck during the movement and does not come back to its neutral point by itself. If this happens during usage, an unwanted movement of the chair could be the result. An unwanted movement could result in damage to the wheelchair, material damage around the chair and/or injury to the user, attendant or by-standers.

Take action

Contact the company

Recalling firmmo-Vis BVBABiebuyckstraat 15D · Nevele, Belgium

✎ GovInfoNow plain-language explainer

mo-Vis BVBA is recalling the Scoot Control R-net device because its throttle lever can get stuck in place instead of returning to neutral. This malfunction can cause the wheelchair to move unexpectedly while in use. The issue poses a risk of injury to users, attendants, or bystanders, as well as potential damage to property. Read more at govinfonow.com/recall/56749-mo-vis-scoot-control-r-net-recall-rare-throttle-stuck.

Source Summary by GovInfoNow · govinfonow.com/recall/56749-mo-vis-scoot-control-r-net-recall-rare-throttle-stuck · Updated October 13, 2026 · FDA enforcement record: FDA #Z-0713-2024

Cite this page

“mo-Vis Scoot Control Recall: Throttle Stuck Hazard.” GovInfoNow, updated October 13, 2026. https://govinfonow.com/recall/56749-mo-vis-scoot-control-r-net-recall-rare-throttle-stuck. Based on FDA recall #Z-0713-2024 (https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-0713-2024%22&limit=1).

The FDA announced on Nov. 28, 2023, that mo-Vis BVBA is recalling the Scoot Control R-net because its throttle lever can get stuck, potentially causing unwanted wheelchair movement and injury. The agency issued recall number Z-0713-2024 for the Class II device.

How to tell if you have it

Brand: mo-Vis
Product: Scoot Control R-net
Product Number: P015-61
UDI-DI: 05407008320119
Lot Numbers: 3304-3317, 3322-3329, 3440-3452, 3569-3618, 3830-3844, 4020-4054, 4170-4176, 4250-4255, 4321-4330
Distribution: Tennessee, Texas
Units affected: 129

The hazard

According to the FDA, the throttle lever may temporarily stick during movement and fail to return to its neutral point. This malfunction could cause unwanted wheelchair movement, resulting in material damage or injury to the user, attendant, or bystanders.

Context

GovInfoNow's records show mo-Vis BVBA has one other recall on record since July 10, 2025, involving timing issues in the IDM-MULTI-R component. Other recent recalls of similar products include Munevo Powered Wheelchair Hands-Free Control Software Issue May Cause Steering Drift (June 19, 2026), WHILL Recalls Wheelchairs Due to Brake Failure Risk (Dec. 29, 2025), and Quantum 4Front 2 Wheelchair: Reminder Pop-Ups May Cause Unexpected Stops (June 25, 2026).

How to tell if you have this one

Check if you have a Scoot Control R-net with Product Number P015-61. Verify the UDI-DI number 05407008320119 and ensure the lot numbers fall within the ranges: 3304-3317, 3322-3329, 3440-3452, 3569-3618, 3830-3844, 4020-4054, 4170-4176, 4250-4255, or 4321-4330.

Brand
mo-Vis
Category
Medical device

Based on the official FDA remedy

What to do — step by step

Stop using the device
Cease use of the recalled Scoot Control R-net immediately to prevent potential injury from unwanted movement.
Contact manufacturer for remedy
Reach out to mo-Vis BVBA to inquire about the specific remedy, as no official remedy details are currently provided in the record.

Where it went and when

Where it was distributed

Distributed in Tennessee and Texas.

FDA distribution: “US States: TN, TX.” States read from FDA’s own wording; “not listed” means the notice does not name it.

States: Tennessee, Texas.

Recall timeline

FDA published this recall 50 days after the firm started it.

Nov 28, 2023Firm started the recall
Jan 11, 2024FDA classified it Class II
Jan 17, 2024Published in FDA’s Enforcement Report

Dates from the agency record only; steps without a date are left out.

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Link to this recall

<a href="https://govinfonow.com/recall/56749-mo-vis-scoot-control-r-net-recall-rare-throttle-stuck">mo-Vis Scoot Control Recall: Throttle Stuck Hazard (GovInfoNow)</a>

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-0713-2024 (November 28, 2023) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for Z-0713-2024 to see it in context.
Plain-language summary written by qwen3.6:35b-a3b on October 13, 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.