Reported May 25, 2022 · Ongoing

Olympus Uretero-reno videoscope, Model No. URF-V2

Olympus Corporation of the Americas

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

What you should do

Stop using the affected lot and contact the recalling firm for the return or refund process. Check the FDA enforcement report for lot-level detail.

Firm contact: Olympus Corporation of the Americas · 3500 Corporate Pkwy · Center Valley, PA · 18034-8229

Is this the product you have?

  • Olympus Uretero-reno videoscope, Model No. URF-V2
Lot codes and dates
    • 1 unit
    • serial number 2825505F UDI 04953170343582
Amount recalled
1

Where it was sold

  • Nationwide
  • AZ

Why it was recalled

The bending section of the URF-V2 may crack, resulting in an abnormal shape or abnormal angulation of the bending section.

This product could cause temporary or reversible health problems — stop using it.

Want the full recall guide?

The guide adds the identifying codes laid out for scanning, symptoms to watch for, a timeline, and news coverage of this recall.

Free recall alerts

Get alerted about new Olympus Corporation of the Americas recalls

One email when a matching recall is published. No account, no cost, unsubscribe in one click.

Where this came from

Source: U.S. Food & Drug Administration (openFDA)

Read the FDA (openFDA device enforcement) notice

Data as of Sep 19, 7:36 PM UTC

RecallNow is not a government agency. Every fact on this page is published by the FDA, USDA or CPSC and links back to their notice.