Drug recall
Brand Name: GlideScope Core 15-inch FHD Model/Catalog Number: 0570-0437 Software Version: Core 15 FHD v1.7 and…
FDA recall event 94547 · Class II · Verathon, Inc.
Key facts
| Event ID | 94547 |
|---|---|
| Recall numbers | Z-2021-2024, Z-2022-2024 |
| Recalling firm | Verathon, Inc. |
| Product type | Devices |
| Products | 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, Brand Name: GlideScope Core 15-inch Monitor Model/Catalog Number: 0570-0404 Product Description: Serialized Monitor |
| Classification | Class II |
| Status | Ongoing |
| Voluntary or mandated | Firm Initiated |
| 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. |
| Initiation date | Apr 29, 2024 |
| Report date | Jun 12, 2024 |
| City | Bothell |
| State | WA |
| Country | United States |
| FEI number | 3022472 |
At a glance
- 1–9 Products in this recall
- 10–99 FDA inspections of this firm (FEI)
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About FDA drug and product recalls
FDA enforcement reports list recalls of drugs, biologics, foods and other FDA-regulated products, classified by the potential health hazard.
Source: U.S. Food and Drug Administration (FDA), Enforcement Reports · Source date: