# FDA recall Z-1510-2024

> **Baxter Healthcare Corporation** · Class II · device recall initiated 2024-03-26.

## Product

Hillrom Welch Allyn Spot Vision Screener VS100, marketed under the following models:    a) SPOT VISION SCREENER,W/O CASE,PLUG2/EUR, VS100-2;   b) SPOT VISION SCREENER,W/O CASE,PLUG4/UK, VS100-4;   c) SPOT VISION SCREENER,W/O CASE,PLUG7/SA, VS100-7;   d) SPOT VISION SCREENER,W/CASE,PLUG2/EUR, VS100S-2;   e) SPOT VISION SCREENER,W/CASE,PLUG4/UK, VS100S-4;   f) SPOT VISION SCREENER,W/CASE,PLUG7/SA, VS100S-7;   g) SPOT VISION SCREENER W/CASE, BRAZIL, VS100S-Z;   h) SPOT VS POWER SUPPLY SET/PLUG2/EUR, 106364;   i) SPOT VS POWER SUPPLY SET/PLUG4/UK, 106366;   j) SPOT VS POWER SUPPLY SET/PLUG7/SA, 106368; for use during vision screening

## Reason for recall

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.

## Distribution

Global, US:  NY, IL

## Key facts

- **Recall number:** Z-1510-2024
- **Recalling firm:** Baxter Healthcare Corporation
- **Classification:** Class II
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2024-03-26
- **Report date:** 2024-04-17

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Deerfield, IL, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-1510-2024

## Citation

> AI Analytics. FDA recall Z-1510-2024. Retrieved 2026-07-26 from https://api.ai-analytics.org/recall/Z-1510-2024. Source: US FDA. Licensed CC0.

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