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Recall data is sourced from official U.S. government agencies (CPSC, FDA, NHTSA, USDA) and processed using AI to improve readability. This site is not affiliated with or endorsed by any government agency. Always refer to the original agency notice for authoritative information.

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Medium RiskFDA Device
Medical Devices/Home Healthcare

mo-Vis BVBA: Scoot Control R-net Recalled for Sticking Throttle and Unwanted Movement

Agency Publication Date: January 11, 2024
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Summary

mo-Vis BVBA is recalling approximately 129 units of the Scoot Control R-net (Product Number P015-61), a device used by attendants to maneuver power wheelchairs. The throttle lever on these units can become temporarily stuck during use and may fail to return to its neutral position. This defect can cause the wheelchair to move unexpectedly, which could lead to collisions, injuries for the user or bystanders, and property damage. Consumers should contact their healthcare provider or the manufacturer immediately to determine if their device is safe to use and to learn about the next steps for correction.

Risk

If the throttle lever remains stuck instead of returning to neutral, the wheelchair may continue to move without the attendant's control. This unintended movement can cause the chair to hit objects or people, potentially resulting in serious injury to the rider, the attendant, or nearby individuals.

What You Should Do

  1. Identify your product by checking for the Scoot Control R-net, Product Number P015-61.
  2. Verify if your unit is affected by checking the lot numbers on the device or its packaging. Affected lot numbers include: 3304-3317, 3322-3329, 3440-3452, 3569-3618, 3830-3844, 4020-4054, 4170-4176, 4250-4255, and 4321-4330. The UDI-DI is 05407008320119.
  3. Immediately stop using the device if you notice the throttle lever is resistant, sticky, or does not automatically snap back to the center position when released.
  4. Contact your healthcare provider or the manufacturer, mo-Vis BVBA, located at Biebuyckstraat 15D, Nevele, Belgium, for further instructions on how to receive a repair or replacement for the affected throttle mechanism.
  5. For additional information or questions, you may contact the FDA's medical device recall line at 1-888-463-6332.

Your Remedy Options

๐Ÿ“‹Other Action

Manufacturer repair or replacement guidance

How to: Contact your healthcare provider or the manufacturer for further instructions and potential refund

Affected Products

Product: Scoot Control R-net
Model / REF:
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

Additional Information

Agency: Food and Drug Administration (FDA)
Event ID: 93556
Status: Active
Manufacturer: mo-Vis BVBA
Sold By: Authorized wheelchair dealers; Medical equipment distributors
Manufactured In: Belgium
Units Affected: 129 units
Distributed To: Tennessee, Texas

Were You Affected by This Recall?

If you or a family member were harmed by this recalled product, you may have legal rights. Consider consulting a consumer protection attorney to understand your options for compensation.

Find an Attorney

This is general information, not legal advice. Go Backs is not a law firm and does not provide legal services.

AI-Enhanced Content: The summary, action steps, and risk assessment on this page were generated by AI from official government recall data to improve readability. This is not legal or medical advice. Always refer to the official agency sources below for authoritative information.

Sources: FDA iRES ยท Raw API Response

openFDA Disclaimer: This recall information is sourced from the openFDA API. Do not rely on openFDA to make decisions regarding medical care. While we make every effort to ensure that data is accurate, you should assume all results are unvalidated. Refer to the openFDA terms of service for more information.