Go Backs
HomeCategoriesStatesCheck Your Home
Go Backs

Track product recalls and safety alerts from CPSC, FDA, NHTSA, and USDA. Stay informed and keep your family safe.

Browse

  • Categories
  • States
  • Check Your Home
  • Risk Levels

Agencies

  • CPSC
  • FDA Food
  • FDA Drug
  • FDA Device
  • FDA Veterinary
  • NHTSA
  • USDA

Company

  • About
  • FAQ
  • Contact
  • Terms of Service
  • Privacy Policy
Buy Me a Coffee

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.

ยฉ 2026 Go Backs. All rights reserved.

Medium RiskFDA Device
Medical Devices/Diagnostic Equipment

Olympus Corporation of the Americas: EVIS EXERA III Video System Centers Recalled for Power Supply Failures

Agency Publication Date: October 11, 2024
Share:
Sign in to monitor this recall

Summary

Olympus Corporation of the Americas is recalling 45 units of the EVIS EXERA III Video System Center Model CV-190 because certain units were assembled with power supply parts that do not meet specifications. This defect can prevent the medical imaging system from starting up properly when needed for procedures. These professional video systems are used in hospitals and clinics for endoscopic diagnosis and treatment and were distributed nationwide across the United States. Owners of affected serial numbers should contact the manufacturer immediately to ensure their equipment is functioning correctly.

Risk

The device may fail to power on or operate during medical procedures due to out-of-specification power supply components. This could lead to procedure delays or interruptions, potentially impacting patient diagnosis or treatment.

What You Should Do

  1. Identify if your device is affected by checking the serial number on the rear or side panel of your EVIS EXERA III Video System Center Model CV-190.
  2. Check if your device matches any of the following 45 serial numbers: 7384484, 7384422, 7384487, 7384478, 7384479, 7384442, 7384441, 7384485, 7384451, 7384455, 7384481, 7384470, 738424, 7384423, 7384489, 7384531, 7384516, 7384492, 7384512, 7384543, 7384483, 7384624, 7384623, 7384497, 7384495, 7384494, 7384533, 7384622, 7384660, 7384654, 7384656, 7384647, 7384658, 7384675, 7384655, 7384704, 7384709, 7384687, 7384706, 7384661, 7384662, 7384703, 7384670, 7384679, or 7384678.
  3. Contact Olympus Corporation of the Americas or your healthcare facility's biomedical engineering department to report affected units and arrange for technical support.
  4. If you have questions regarding the status of your equipment or next steps for repair, contact the manufacturer directly at 1-800-848-9024 or through their website.
  5. For additional information or to report a related issue, contact the FDA at 1-888-463-6332 or visit www.fda.gov/medical-devices/medical-device-recalls.

Your Remedy Options

๐Ÿ“‹Other Action

Manufacturer correction/repair

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

Affected Products

Product: EVIS EXERA III Video System Center CV-190
Model / REF:
CV-190
UPC Codes:
04953170298622
Lot Numbers:
7384484
7384422
7384487
7384478
7384479
7384442
7384441
7384485
7384451
7384455
7384481
7384470
7384424
7384423
7384489
7384531
7384516
7384492
7384512
7384543
7384483
7384624
7384623
7384497
7384495
7384494
7384533
7384622
7384660
7384654
7384656
7384647
7384658
7384675
7384655
7384704
7384709
7384687
7384706
7384661
7384662
7384703
7384670
7384679
7384678

Additional Information

Agency: Food and Drug Administration (FDA)
Event ID: 93217
Status: Active
Manufacturer: Olympus Corporation of the Americas
Sold By: Olympus Corporation of the Americas
Manufactured In: United States
Units Affected: 45 units
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.