FDA Warns Medline Beds Pose Fire and Entrapment Risks

The U.S. Food and Drug Administration has issued an alert about Medline electric beds used in homes and long-term care facilities. The agency cited at least two deaths and 16 serious injuries associated with the beds and related products, based on information Medline had as of October 20.

The beds’ electrical parts can overheat, particularly under certain conditions such as a jammed motor or component. This can cause smoke, melting, burning or fire, and may also expose users to electrical shock or burns. Accessories including mattresses, side rails and bed kits may create entrapment or asphyxiation risks.

Medline, based in Northfield, Illinois, has told customers to modify the products before continued use and advised vendors to stop selling the beds and related equipment. The company is discontinuing its residential and extended-care bed lines and related products, and withdrawing from that business. It said the decision prioritizes safety and that it is working to support affected customers and health care providers.

Medline says owners should plug in the beds only when repositioning a patient and should not use extension cords. Some beds may be repairable; those that cannot be repaired may qualify for a refund or replacement. Customers can contact Medline’s recall service at 800-950-0128, option 7. The FDA said it is reviewing the issue and will share significant updates.