# FDA recall Z-2022-2024

> **Verathon, Inc.** · Class II · device recall initiated 2024-04-29.

## 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.

## Distribution

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

## Key facts

- **Recall number:** Z-2022-2024
- **Recalling firm:** Verathon, Inc.
- **Classification:** Class II
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2024-04-29
- **Report date:** 2024-06-12

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Bothell, WA, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-2022-2024

## Citation

> AI Analytics. FDA recall Z-2022-2024. Retrieved 2026-07-26 from https://api.ai-analytics.org/recall/Z-2022-2024. Source: US FDA. Licensed CC0.

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