# FDA recall Z-1509-2024

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

## Product

Hillrom Welch Allyn Connex ProBP 3400 Digital Blood Pressure Device, marketed under the following models:    a) PROBP 3400, SUREBP, BLUETOOTH, MOBILE,EU, Product Code 34BFST-2;   b) PROBP 3400, SUREBP, BLUETOOTH, MOBILE,UK, Product Code 34BFST-4;   c) PROBP 3400, SUREBP, BLUETOOTH, MOBILE,AU, Product Code 34BFST-6;   d) PROBP 3400, BLUETOOTH, MOBILE, EU, Product Code 34BXST-2;   e) PROBP 3400, BLUETOOTH, MOBILE, UK, Product Code 34BXST-4;   f) PROBP 3400, BLUETOOTH, MOBILE, ZA, Product Code 34BXST-7;   g) PROBP 3400, SUREBP, MOBILE, EU, Product Code 34XFST-2;   h) PROBP 3400, SUREBP, MOBILE, UK, Product Code 34XFST-4;   i) PROBP 3400, SUREBP, MOBILE, AU, Product Code 34XFST-6;   j) PROBP 3400, SUREBP, MOBILE, ZA, Product Code 34XFST-7;   k) PROBP 3400, MOBILE, EU, Product Code 34XXST-2;   l) PROBP 3400, MOBILE, UK, Product Code 34XXST-4;   m) PROBP 3400, MOBILE, AU, Product Code 34XXST-6;   n) PROBP 3400, MOBILE, ZA, Product Code 34XXST-7;   o) PROBP MOBILE STAND CORD ASSY EUROPE, Prod

## 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-1509-2024
- **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-1509-2024

## Citation

> AI Analytics. FDA recall Z-1509-2024. Retrieved 2026-06-25 from https://api.ai-analytics.org/recall/Z-1509-2024. Source: US FDA. Licensed CC0.

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