Verathon, Inc. recalls Brand Name: GlideScope Core 15-inch FHD Model/Catalog Number: 0570-0437 Software Version: Core 15 FHD v1.7 and earlier…

Recall date

April 29, 2024

Source

U.S. Food & Drug Administration (FDA) — enforcement report

Recall number

Z-2022-2024

FDA classification

Class II

Brand / firm

Verathon, Inc.

Sold / distributed

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

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.

Class II means using this product may cause temporary or medically reversible health problems; the chance of serious harm is remote.

What was recalled

Brand Name: GlideScope Core 15-inch FHD Model/Catalog Number: 0570-0437 Software Version: Core 15 FHD v1.7 and earlier Product Description: Serialized Monitor