FDA Medical devices recall ·
MEDLINE beds labeled as: Semi Electric Lightweight Homecare Bed recall
This is an FDA Class I recall — the most serious type.
- Recall number
- Z-1012-2026
- Date
- (initiated November 26, 2025)
- Company / brand
- Medline Industries, LP
3 Lakes Dr, Northfield, IL, United States - Category
- Medical devices › Class I
- Classification
- Class I
- Status
- Ongoing
- Units affected
- 13245 units
- Hazard tags
- Fire Burn
- Initiated by
- Voluntary: Firm initiated
Read the official FDA notice ↗
Product
MEDLINE beds labeled as: Semi Electric Lightweight Homecare Bed, REF MDR107002L
Why was it recalled?
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 should you do?
FDA enforcement reports do not list a consumer remedy. Check the product codes below against what you have; if it matches, stop using it and follow the instructions in the firm's or FDA's official notice, or contact the company. If you have health concerns, contact your healthcare provider.
Product codes & lot numbers
UDI/DI 40080196294320, All lots
Distribution
US, CA, PA, GUAM, VI
States: California Pennsylvania
What does Class I mean?
Class I is the most serious FDA recall class: there is a reasonable probability that using or being exposed to the product will cause serious adverse health consequences or death.
Source: FDA (medical devices), recall Z-1012-2026. Official notice. Republished from public data; RecallFlag is not affiliated with the FDA.