Verathon, Inc.: Device Recall
Recall #Z-2021-2024 · 04/29/2024
Class II: Risk
Recall Details
- Recall Number
- Z-2021-2024
- Classification
- Class II
- Product Type
- Device
- Recalling Firm
- Verathon, Inc.
- Status
- Ongoing
- Date Initiated
- 04/29/2024
- Location
- Bothell, WA, United States
- Voluntary/Mandated
- Voluntary: Firm initiated
- Product Quantity
- 2568 devices
Reason for Recall
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.
Product Description
Brand Name: GlideScope Core 15-inch Monitor Model/Catalog Number: 0570-0404 Product Description: Serialized Monitor
Distribution Pattern
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
Other Recalls by Verathon, Inc.
- Class II: Risk 04/29/2024
Data from FDA openFDA enforcement reports. This site is not affiliated with or endorsed by the FDA. Recall information may be updated by the FDA at any time.