FDA Device recall Z-2021-2024
Brand Name: GlideScope Core 15-inch Monitor Model/Catalog Number: 0570-0404 Product Description: Serialized Monitor
- FDA Device
- Class II
- ongoing
- Published 2024-06-12
On 2024-06-12 the FDA classified a Class II recall of Brand Name: GlideScope Core 15-inch Monitor Model/Catalog Number: 0570-0404 Product Description: Serialized Monitor by Verathon, citing 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.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-2021-2024 |
| Classification | Class II |
| Status | ongoing |
| Initiated | 2024-04-29 |
| Published | 2024-06-12 |
| Last updated | 2026-09-13 11:57 UTC |
| Company | Verathon |
| Distribution | 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, OR, PA, RI, SC, SD, TN, TX, UT, VA, WA, WI, WV, WY |
Product
Brand Name: GlideScope Core 15-inch Monitor Model/Catalog Number: 0570-0404 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.
Identifiers
| code_info | Software Version: v1.9 and earlier/ UDI: UDI/DI: 00879123006639 |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:57 UTC. Current status: ongoing.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2021-2024%22
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