ProductGuru Recalls

Official recall record

MEDLINE beds labeled as: Full Electric Lightweight Homecare Bed, REF MDR107003L

US FDA — Medical Devices · 2025-11-26 · United StatesClass I
Issuing authority
US FDA — Medical Devices
Recall initiated by firm
2025-11-26
Country of alert
United States
Alert level
Class I
Alert type
recall
Barcode (EAN/GTIN)
40080196294344
Brand on record
Medline Industries, LP
Product category
Medical Device

What the authority reported

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.

What to do

Follow the instructions in the official notice — recall remedies (refund, repair, replacement, or disposal) are defined by the issuing authority and the responsible business, and they differ per recall. Do not rely on summaries, including this one.

Verify at the source: US FDA — Medical Devices — official record →
Record last checked against the registry on 2026-05-31.

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Other recalls from this brand

All 257 official recall notices naming Medline Industries, LP on this site →

ProductGuru Recalls republishes official safety information with attribution. We are not the issuing authority and this page is not advice. If this product is a medical device or medication, speak to a doctor or pharmacist. Found an error? Report it — corrections are published.