Welch Allyn recalls VS100 Spot Vision Screener software version 3.2.0.1 due to potential flickering that could trigger photosensitive seizures in susceptible individuals. Affected units sold with specific model and software version.
Display screen may unintentionally flicker due to a software issue. Exposure to flickering lights may induce photosensitive seizure activity in susceptible individuals.
Welch Allyn is recalling its Spot Vision Screener VS100 device because a software issue might cause the screen to flicker, which could trigger photosensitive seizures in some people. This recall affects specific software versions of the device.
The software issue causes the screen to flicker unintentionally. Flickering lights can trigger photosensitive seizures in people who are particularly sensitive to such visual patterns.
People who own or use the Welch Allyn Spot Vision Screener VS100 with software version 3.2.0.1 are affected. Those with photosensitive epilepsy or a history of seizures are at higher risk.
Check if your device has software version 3.2.0.1. The product is sold under Welch Allyn, model VS100, with specific packaging details listed in the recall notice.
Look for the software version on your device; affected units have version 3.2.0.1.
The recall states that the software issue may cause flickering that could trigger seizures in susceptible individuals, so it's recommended to check the software version and take action if needed.
Check if your device has software version 3.2.0.1. If it does, contact Welch Allyn for instructions on how to proceed.
Affected units have software version 3.2.0.1 and are sold under Welch Allyn as the Spot Vision Screener VS100 model.
We’ve drafted a message you can send Welch Allyn to request your refund or repair — edit it as you like.
Subject: Recall Z-1573-2026 — Welch Allyn Welch Allyn Hello, I own a Welch Allyn that is covered by recall Z-1573-2026 from Welch Allyn. 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.
