Class III — Low Risk

Low risk — use of or exposure to this product is not likely to cause adverse health consequences.

GlideScope Go Monitors Recalled by Verathon, Inc. Due to Handheld video monitor failed to meet the labeled...

Date: July 1, 2021
Company: Verathon, Inc.
Status: Ongoing
Source: FDA (Device)

What You Should Do

Stop using this product immediately. Do not consume, use, or distribute it.

Return the product to the place of purchase for a full refund. If you have questions, contact Verathon, Inc. directly.

Affected Products

GlideScope Go Monitors

Quantity: 8,569

Why Was This Recalled?

Handheld video monitor failed to meet the labeled IP67 rating which may allow fluid ingress into the monitor resulting in loss of functionality.

Where Was This Sold?

This product was distributed nationwide across all 50 states.

Affected (51 states)Not affected

About Verathon, Inc.

Verathon, Inc. has 13 total recalls tracked by RecallDetector.

Related Recalls

Data sourced from the FDA (Device). Last updated March 26, 2026. View original report