MEDLINE beds labeled as: Semi Electric Lightweight Homecare Bed, REF MDR107002L
Summary
The FDA issued a Class I for MEDLINE beds labeled as: Semi Electric Lightweight Homecare Bed, REF MDR107002L by Medline Industries, LP. Reason: Medline Industries has identified a potential hazard involving the hand control pendant and associated wires. In rare and atypical scenarios such as o.
Details
Source
Device Recall
External ID
Z-1012-2026
Action Date
2026-01-28
Status
Ongoing
Category
device
Product Description
MEDLINE beds labeled as: Semi Electric Lightweight Homecare Bed, REF MDR107002L
Lot/Code Info: UDI/DI 40080196294320, All lots
Quantity Affected: 13245 units
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
Type: Voluntary: Firm initiated
Recall Initiated: 2025-11-26
Company
Northfield, IL
Context & Analysis
This is a Class I recall. Class I recalls are the most serious — there is a reasonable probability that use of or exposure to the product will cause serious health consequences or death.
This was one of 180 device recalls issued in the same week, part of 413 device-related FDA actions this month.
Medline Industries, LP has 442 FDA actions in our database, including 415 recalls and 27 clearances.
Frequently Asked Questions
What is a Class I recall?
A Class I recall is the most serious type. The FDA has determined there is a reasonable probability that the product will cause serious adverse health consequences or death. Consumers should stop using the product immediately.
What should I do if I have this product?
Stop using the product. Check the product against the specific lot numbers or identifiers listed in the recall. Contact the manufacturer (Medline Industries, LP) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.
How often does Medline Industries, LP have FDA actions?
Medline Industries, LP has 442 FDA actions in our database, including 415 recalls and 27 device clearances.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "Z-1012-2026" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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