# FDA recall Z-1511-2024

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

## Product

Power Cords, marketed under the following models:    a) CORD,METAL EARTH PIN, 2.5A,250V,2.5M,C7, 714682;   b) PLFM CLASS II POWER CORD - AUSTRALIA, 716010;   c) PLFM CLASS II POWER CORD -  EUROPE, 716012;   d) POWER CORD,AUSTRALIA,2.5A,250V,2.5M,C7, 008-0910-00;   e) POWER CORD,EUROPEAN,2.5A,250V,2.5M,C7, 008-0912-00;   f) LINE CORD (EURO), 4500-402;   g) LINE CORD (UK), 4500-404;   h) LINE CORD (AUS), 4500-406

## 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-1511-2024
- **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-1511-2024

## Citation

> AI Analytics. FDA recall Z-1511-2024. Retrieved 2026-07-29 from https://api.ai-analytics.org/recall/Z-1511-2024. Source: US FDA. Licensed CC0.

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