Medline Industries recalled 22,565 Full Electric Low Basic Homecare Beds on November 26, 2025, due to a fire risk. The recall affects beds labeled with REF MDR107003ELO following 58 reports of overheating hand control pendants. Consumers should stop using the beds and follow recall instructions immediately.
Quick Facts at a Glance
Recall Date
November 26, 2025
Hazard Level
HIGH
Brand
Medline Industries, LP
Category
Health & Personal Care
Sold At
Multiple Retailers
Geographic Scope
3 states
At-Risk Groups
GENERAL
Hazard Information
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 You Should Do
Patients and healthcare providers should stop using this device immediately. Follow the recall instructions provided by the manufacturer. Contact Medline Industries, LP or your healthcare provider for instructions. Notification method: Letter
Get instant alerts for Health & Personal Care recalls
Be the first to know. Free instant alerts to your inbox.
No spamUnsubscribe anytime
About This Product
The Full Electric Low Basic Homecare Bed is designed for patient comfort and mobility in homecare settings. Consumers buy this product to provide a safe and adjustable sleeping environment for individuals with limited mobility.
Why This Is Dangerous
The hazard arises from the potential for the hand control pendant and wires to overheat, which can occur if the bed is misused or obstructed. This overheating can lead to serious fire risks, including sparking and burning.
Industry Context
This recall is not part of a broader industry pattern.
Real-World Impact
Consumers must stop using the affected beds to prevent fire hazards. This may create inconvenience for users who rely on these beds for medical needs.
Practical Guidance
How to identify if yours is affected
Verify if the model matches REF MDR107003ELO.
Check for any signs of damage on the pendant or wires.
Review any communication from Medline regarding the recall.
Where to find product info
The model number is typically found on the bed's frame or under the mattress.
What timeline to expect
Expect 4-6 weeks for refund processing after returning the bed.
If the manufacturer is unresponsive
Follow up with Medline Industries via phone or email.
File a complaint with the CPSC if necessary.
How to prevent similar issues
Always check for recalls before purchase.
Ensure proper use according to the manufacturer's guidelines.
Inspect medical devices regularly for wear and tear.
Documentation advice
Keep records of your purchase, any communications with Medline, and photos of the product for your records.
Product Details
The recalled product is the Full Electric Low Basic Homecare Bed, REF MDR107003ELO. A total of 22,565 units were distributed across the United States, Canada, Puerto Rico, Guam, and the Virgin Islands. These beds were sold through various healthcare providers.
Reported Incidents
Medline Industries received 58 complaints involving incidents of pendant sparking, burning, melting, or smoking. Fortunately, no injuries or deaths have been reported.
Key Facts
Recall date: November 26, 2025
Model: Full Electric Low Basic Homecare Bed, REF MDR107003ELO
Medline Industries, LP recalled 60 medical convenience kits worldwide due to a potential rotating adaptor unwinding in NAMIC Angiographic RA control syringes. The issue may cause a loose connection or disconnection between the syringe and manifold. Healthcare providers should stop using the device and follow the manufacturer’s recall instructions.
Medline Industries, LP recalled 439 medical convenience kits containing NAMIC Angiographic Rotating Adaptor syringes. The recall spans worldwide distribution including the US, Puerto Rico, and multiple international markets.
Medline Industries, LP recalls 762 medical convenience kits containing NAMIC Angiographic Rotating Adaptor syringes sold worldwide, including the U.S., PR, Canada, and several international markets. The recall cites a potential risk that the syringe rotating adaptor may unwind during use, creating a loose connection or disconnect between the syringe and the manifold. Stop using the device and seek
Medline Industries, LP recalls 17,902 medical convenience kits worldwide after post-market surveillance found a potential risk of the syringe rotating adaptor unwinding. The recall covers NAMIC Angiographic RA control syringes labeled in 10 Medline SKUs. Healthcare providers should stop use immediately and follow recall instructions.
Medline Industries issued a Class I recall for 79,843 medical convenience kits containing NAMIC Angiographic Rotating Adaptor syringes. The action covers worldwide distribution including the US and PR. The risk is a syringe adaptor unwinding during use, which may cause a loose connection or disconnection with the manifold. Stop using the device immediately and follow recall instructions.
Medline Industries recalls 192,690 Angiographic Control Syringes worldwide after post-market surveillance found a rotating adaptor may unwind. The defect can cause a loose or complete disconnection between syringe and manifold. Stop using immediately and follow recall instructions.
Medline Industries, LP recalls 3,120 medical convenience kits worldwide due to a risk the syringe rotating adaptor may unwind during use. The issue can create a loose connection or complete disconnection between the syringe and manifold. The recall was issued on February 27, 2026 and is active. Customers should stop using the kit and follow manufacturer instructions for recall notices.
Medline Industries, LP recalls 1,698 medical convenience kits worldwide over a potential unwind of the NAMIC Angiographic Rotating Adaptor during use. The risk could cause a loose connection or complete disconnection between the syringe and manifold. Healthcare providers and patients should stop using the affected kits immediately and follow recall instructions.