Recall Z-2022-2024— Verathon, Inc.
Class II · Ongoing
Class II FDA medical device recall by Verathon, Inc., initiated 2024-04-29. FDA's recall record names no specific 510(k) clearance for this event. Product: 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. Reason: 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..
- Recalling firm
- Verathon, Inc.
- Classification
- Class II
- Status
- Ongoing
- Initiated
- 2024-04-29
- Firm location
- Bothell, WA, United States
Product description
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
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.
Data sourced from openFDA. This site is unofficial and independent of the FDA.