# FDA recall Z-0033-2025

> **MEDLINE INDUSTRIES, LP - Northfield** · Class II · device recall initiated 2024-08-30.

## Product

MEDLINE AUTOMATIC DIGITAL BLOOD PRESSURE UNIT, REF MDS1001U.

## Reason for recall

It has been determined that certain Blood Pressure Monitors containing a faulty microchip have failed to power on or have shown display screen issues after the initial few uses, as well as overheating at times making the unit warm to the touch.

## Distribution

Worldwide distribution - US Nationwide and the countries of Panama and Jamaica.

## Key facts

- **Recall number:** Z-0033-2025
- **Recalling firm:** MEDLINE INDUSTRIES, LP - Northfield
- **Classification:** Class II
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2024-08-30
- **Report date:** 2024-10-16

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

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-0033-2025

## Citation

> AI Analytics. FDA recall Z-0033-2025. Retrieved 2026-06-25 from https://api.ai-analytics.org/recall/Z-0033-2025. Source: US FDA. Licensed CC0.

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