Reported Apr 17, 2024 · Ongoing

Hillrom Welch Allyn Spot Vision Screener VS100, marketed under the following models

Baxter Healthcare Corporation

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

What you should do

Stop using the affected lot and contact the recalling firm for the return or refund process. Check the FDA enforcement report for lot-level detail.

Firm contact: Baxter Healthcare Corporation · 1 Baxter Pkwy · Deerfield, IL · 60015-4625

Is this the product you have?

Hillrom Welch Allyn Spot Vision Screener VS100, marketed under the following models

10 of 10 products

Products covered by this recall
#Product as published
1SPOT VISION SCREENER,W/O CASE,PLUG2/EUR, VS100-2
2SPOT VISION SCREENER,W/O CASE,PLUG4/UK, VS100-4
3SPOT VISION SCREENER,W/O CASE,PLUG7/SA, VS100-7
4SPOT VISION SCREENER,W/CASE,PLUG2/EUR, VS100S-2
5SPOT VISION SCREENER,W/CASE,PLUG4/UK, VS100S-4
6SPOT VISION SCREENER,W/CASE,PLUG7/SA, VS100S-7
7SPOT VISION SCREENER W/CASE, BRAZIL, VS100S-Z
8SPOT VS POWER SUPPLY SET/PLUG2/EUR, 106364
9SPOT VS POWER SUPPLY SET/PLUG4/UK, 106366
10SPOT VS POWER SUPPLY SET/PLUG7/SA, 106368; for use during vision screening
Lot codes and dates

10 of 10 products

Products covered by this recall
#BarcodesProduct as published
1732094224214VS100-2, UDI/DI 732094224214
2732094224191VS100-4, UDI/DI 732094224191
3732094224092VS100-7, UDI/DI 732094224092
4732094224177VS100S-2, UDI/DI 732094224177
5732094224153VS100S-4, UDI/DI 732094224153
6732094224085VS100S-7, UDI/DI 732094224085
7732094294217VS100S-Z, UDI/DI 732094294217
8732094246964106364, UDI/DI 732094246964
9732094319927106366, UDI/DI 732094319927
10732094248692106368, UDI/DI 732094248692
Amount recalled
3547 units

This recall covers 3 products

The agency filed one notice per product. You are reading one of them; the other 2 are below.

Where it was sold

Why it was recalled

Baxter received reports of an issue related to the construction of the power cord not meeting the insulation rating per country-specific requirements and international electrical standards.

This product could cause temporary or reversible health problems — stop using it.

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Where this came from

Source: U.S. Food & Drug Administration (openFDA)

Read the FDA (openFDA device enforcement) notice

Data as of Sep 19, 6:21 PM UTC

RecallNow is not a government agency. Every fact on this page is published by the FDA, USDA or CPSC and links back to their notice.