FDA Device recall Z-1013-2026

MEDLINE beds labeled as: 1) Full Electric Basic Homecare Bed, REF MDR107003E

• FDA Device
• Class I
• ongoing
• Published 2026-01-28

On 2026-01-28 the FDA classified a Class I recall of MEDLINE beds labeled as: 1) Full Electric Basic Homecare Bed, REF MDR107003E by Medline Industries, citing 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 sp….

Read the official FDA Device notice

Product

MEDLINE beds labeled as: 1) Full Electric Basic Homecare Bed, REF MDR107003E; 2) Full Electric Basic Homecare Bed, 4-pack,REF MDR107003E-4.

Reason

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.

Identifiers

Status history

No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:58 UTC. Current status: ongoing.

Source

Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-1013-2026%22

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