FDAFDA · Food and drugs·Recall number Z-2021-2024
Brand Name: GlideScope Core 15-inch Monitor Model/Catalog Number: 0570-0404 Product Description: Serialized Monitor
Published June 12, 2024 · Recall initiated: April 29, 2024
Status when published: Ongoing — openFDA updates weekly, so this field may not reflect the current status. Always confirm with the official notice.
What's the hazard
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.
What to do
Voluntary: Firm initiated · Letter
Recall details
- Manufacturer
- Verathon, Inc.
- Distributor
- 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
- Lot
- Software Version: v1.9 and earlier/ UDI: UDI/DI: 00879123006639
- Risk classification
- Class II
- Area (FDA)
- device
- Country
- United States
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