# FDA recall Z-1012-2026

> **Medline Industries, LP** · Class I · device recall initiated 2025-11-26.

## Product

MEDLINE beds labeled as: Semi Electric Lightweight Homecare Bed, REF MDR107002L

## Reason for recall

Medline Industries has identified a potential hazard involving the hand control pendant and associated wires. In rare and atypical scenarios such as operating the bed above its specified weight limit, encountering an obstruction to bed movement, or experiencing jammed components/motor the hand pendant and pendant cords may overheat and, in rare instances, pose a risk of fire.  Medline Industries, LP has received a total of (58) complaints associated with reports of pendant sparking, burning, melting, smoking or fire.

## Distribution

US, CA, PA, GUAM, VI

## Key facts

- **Recall number:** Z-1012-2026
- **Recalling firm:** Medline Industries, LP
- **Classification:** Class I
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2025-11-26
- **Report date:** 2026-01-28

- **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-1012-2026

## Citation

> AI Analytics. FDA recall Z-1012-2026. Retrieved 2026-06-08 from https://api.ai-analytics.org/recall/Z-1012-2026. Source: US FDA. Licensed CC0.

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