Reported Jun 12, 2024 · Ongoing

Brand Name: GlideScope Core 15-inch Monitor Model/Catalog Number: 0570-0404 Product Description: Serialized Monitor

Verathon, Inc.

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: Verathon, Inc. · 20001 N Creek Pkwy · Bothell, WA · 98011-8218

Is this the product you have?

  • Brand NameGlideScope Core 15-inch
  • Monitor Model/Catalog Number0570-0404
  • Product DescriptionSerialized Monitor
Lot codes and dates
  • Software Versionv1.9
  • and earlier/ UDIUDI/DI: 00879123006639
Amount recalled
2568 devices

This recall covers 2 products

The agency filed one notice per product. You are reading one of them; the other one is below.

Where it was sold

Why it was recalled

Due to software issues, their is the potential for loss of image or a degradation of the image when using the monitor with other connectable devices.

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 Verathon, Inc. 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, 5:43 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.