FDA Recall: Potential for Loss or Degradation of Image When Using Monitor with other Devices

Company: Verathon, Inc.
Date of Enforcement Report: 6/4/2024
Class II

PRODUCT

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

Recall Number:

Z-2021-2024

REASON:

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

RECALLING FIRM/MANUFACTURER:

Verathon, Inc.

VOLUME OF PRODUCT IN COMMERCE:

2568 devices

DISTRIBUTION:

US: AK AL AR AZ CA CO CT DC FL GA HI IA ID IL IN KS KY LA MA MD ME MI MN MO MS MT NC ND NE NH NJ NM NV NY OH OK ON OR PA QLD RI SC SD TN TX UT VA VIC WA WI WV WY OUS: Hong Kong, Indonesia, Saudi Arabia

About the author

Allison joined SoftwareCPR in 2022, bringing along over ten years of passion for building teamwork and growth in organizations. This is established in part by the greatest University the South has to offer- Mississippi State.

Upcoming Public Courses

IEC 62304 and Emerging Standards Impacting Medical Device and HealthIT Software training course in Boise, Idaho. 3-Day course.

October 13-15, 2026

Limited Early Bird Registration: $995 / person
Non refundable but transferable.

Or just email training@softwarecpr.com for more info.

Corporate Office

15148 Springview St.
Tampa, FL 33624
USA
+1-781-721-2921
Partners located in the US (CA, FL, MA, MN, TX) and Canada.