Verathon recalls GlideScope Core 15-inch FHD monitors with software v1.7 and earlier due to potential image loss or degradation when connected to other devices. Affected units may require software updates to prevent issues.
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.
Verathon is recalling GlideScope Core 15-inch FHD monitors with software version v1.7 and earlier because they can lose or degrade images when connected to other devices. This could affect medical imaging systems where clear visuals are critical.
The software issues can cause image loss or degradation when the monitor connects with other devices. This might lead to unclear medical images, but it does not cause physical harm or system failure.
Healthcare providers using GlideScope monitors with software versions v1.7 and earlier are most at risk, particularly those in settings where image clarity is essential for diagnosis.
Check for the model number 0570-0437 and software version v1.7 or earlier on the monitor. The product was sold with a unique identifier starting with 00879123008596.
Verify the software version on your monitor; affected units have v1.7 or earlier.
No, the recall involves potential image loss or degradation when connecting to other devices, but it does not cause physical harm or system failure.
Check for model number 0570-0437 and software version v1.7 or earlier on the monitor.
The recall does not specify a remedy, so contact Verathon directly for guidance.
We’ve drafted a message you can send Verathon to request your refund or repair — edit it as you like.
Subject: Recall Z-2022-2024 — Verathon Verathon Hello, I own a Verathon that is covered by recall Z-2022-2024 from Verathon. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
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The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
