Brand Name: GlideScope Core 15-inch FHD Model/Catalog Number:… — Class II medical device recall Z-2022-2024
Ongoing recall by Verathon, Inc., reported 2024-06-12, distributed in AK, AL, AR, AZ, CA, CO, CT, DC…. Due to software issues, their is the potential for loss of image or a degradation of the image when using the
| Recall number | Z-2022-2024 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Ongoing |
| Voluntary or mandated | Voluntary |
| Recalling firm | Verathon, Inc., Bothell, WA, United States |
| Recall initiated | 2024-04-29 |
| Classified | 2024-06-04 |
| Reported by FDA | 2024-06-12 |
| Distributed | 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, RI, SC, SD, TN, TX, UT, VA, WA, WI, WV, WY |
| Countries outside the US | HK, ID, SA |
| Quantity | 1,706 devices |
| Reason classes | specification failure, software |
| UPC / GTIN / UDI-DI | 00879123008596 |
| Model numbers | 0570-0437 |
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 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.
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/Z-2022-2024. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.