Product Wiki · Recalls · U.S. FDA — Device Enforcement

Recall Z-1015-2026 — MEDLINE beds labeled as: Full Electric Lightweight Homecare Bed, REF MDR107003L

U.S. FDA — Device Enforcement · United States · 2025-11-26 · Class I

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Agency
U.S. FDA — Device Enforcement
Recall identifier
Z-1015-2026
Date of alert
2025-11-26
Country / jurisdiction
United States
Risk level
Class I
Risk type
recall
Brand
Medline Industries, LP
Product category
device
Product type
Devices
Barcode (EAN/GTIN)
40080196294344
Reported risk: 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.
Primary source: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts

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ProductGuru indexes recall and safety-alert records from ~30 public agency registries. We are not lawyers, regulators or product-safety consultants. This page restates what the named agency published; consult the primary source above (or qualified counsel in your jurisdiction) before any commercial, medical or safety decision.