MEDLINE beds labeled as: Full Electric Low Lightweight recall
MEDLINE beds labeled as: Full Electric Low Lightweight Homecare Bed, REF MDR107003LO
Why was MEDLINE beds labeled as: Full Electric Low Lightweight 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 I do if I have this product?
The recall is ongoing. Follow the firm and FDA instructions.
What to do with a recalled product: refunds, receipts, safe disposal and how to report a problem.
Is my product affected?
Compare the item in your hand with every identifier below from the official FDA record. Only products that match the listed product and lot, UPC or model codes are part of this recall.
Which lot codes, UPCs or models are affected?
UDI/DI 40080196325901, All lots
- Product
- MEDLINE beds labeled as: Full Electric Low Lightweight Homecare Bed, REF MDR107003LO
- Recalling firm
- Medline Industries, LP
- Quantity
- 15581 units
- Distribution
- US, CA, PA, GUAM, VI
- Recall date
- January 28, 2026
- Classification
- Class I
- Status
- Ongoing
- Agency
- FDA (device)