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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/Diagnostic Equipment

EVIDENT SCIENTIFIC INC: SlideView VS200 Slide Viewer Recalled Due to Shutter and Laser Malfunction

Agency Publication Date: July 26, 2024
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Summary

Evident Scientific Inc. is recalling SlideView VS200 slide viewers because a badly positioned internal cable can cause a short circuit. This short circuit destroys a fuse inside the laser, causing the shutter to remain stuck in either an open or closed position and making the device impossible to operate. This recall is mandated by the FDA and affects units distributed throughout the United States.

Risk

A short circuit in the door control system can result in a laser shutter that fails to close or open. This malfunction prevents the device from working properly and could lead to unexpected equipment failure or potential laser exposure issues if the shutter remains open during maintenance.

What You Should Do

  1. Identify your device by checking the product label for 'SlideView VS200 slide viewer' and one of the following identifying codes: 65159, 67105, 67104, 69153, 67106, or 69154.
  2. Verify if your unit is affected by locating the Recall Number Z-2416-2024 associated with your equipment.
  3. If your device's laser shutter has stopped responding or is stuck in one position, contact your healthcare provider or Evident Scientific Inc. for technical support and further instructions.
  4. Contact Evident Scientific Inc. at their Waltham, Massachusetts headquarters or via their official website for details on how to receive a repair or corrective action for the mispositioned cable and blown fuse.
  5. For additional questions or to report further issues, contact the FDA at 1-888-463-6332 (1-888-INFO-FDA).

Your Remedy Options

๐Ÿ“‹Other Action

Contact manufacturer for repair or guidance

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

Affected Products

Product: SlideView VS200 slide viewer
Model / REF:
65159
67105
67104
69153
67106
69154

Additional Information

Agency: Food and Drug Administration (FDA)
Event ID: 95028
Status: Active
Manufacturer: EVIDENT SCIENTIFIC INC
Sold By: authorized medical device distributors
Manufactured In: United States
Distributed To: Nationwide

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.