Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Invacare¿ Foot Section for Semi & Full Electric Beds Recalled by Invacare Corporation Due to The firm recently identified a quality issue with...
What You Should Do
Stop using this product immediately. Do not consume, use, or distribute it.
Return the product to the place of purchase for a full refund. If you have questions, contact Invacare Corporation directly.
Affected Products
Invacare¿ Foot Section for Semi & Full Electric Beds, Junction Boxes, Product Usage: The Invacare Bariatric home care bed is intended to provide a rest surface with adjustable height from floor and adjustable surface contours.
Quantity: 3,050 units
Why Was This Recalled?
The firm recently identified a quality issue with the Junction box used in the Invacare Bariatric Bed. They discovered that the Junction Box may omit sparks which could result in a fire in the presence of flammable materials.
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About Invacare Corporation
Invacare Corporation has 37 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report