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Olympus Corporation of the Americas 2024-10-23 Health serious FDA
Health · FDA · Recall #FDA-Z-0056-2025

EVIS EXERA III Video System Center Model Number CV-190. Intended to be used with OLYMPUS… Recall

Issued October 23, 2024 · Olympus Corporation of the Americas

In October 2024, Olympus Corporation of the Americas recalled the EVIS EXERA III Video System Center Model Number CV-190. Intended to be used with OLYMPUS…, a serious health recall reported by the FDA. Affected owners are eligible for a voluntary. Here is what the hazard is and exactly what to do about it.

Compiled by Maya Ellison, RecallCheckr

What this means for you

Certain serial numbers of the CV-190 do not start up properly because parts that deviated from the specification were assembled into the power supply unit.

What you should do

  1. 1 Stop using EVIS EXERA III Video System Center Model Number CV-190. Intended to be used with OLYMPUS… right away.
  2. 2 Set it aside where it won't be used by mistake.
  3. 3 Contact Olympus Corporation of the Americas to arrange your voluntary. See the official notice below for contact details.
  4. 4 Keep the product until your remedy is fully processed. You may need it.
Official remedy (Voluntary):

Recall details

Brand
Olympus Corporation of the Americas
Category
Health
Recall date
October 23, 2024
Units affected
Not reported
Sold at
US Nationwide distribution.
Recall number
FDA-Z-0056-2025
Made in
United States
Issuing agency
FDA

In context

  • Olympus Corporation of the Americas has 42 recalls in our database, including 6 rated Critical.
  • We're tracking 3,576 Health recalls in our database.
  • This is the 737th Health recall we've logged in 2024.
Read the official FDA notice

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