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Invacare Corporation recalls Invacare¿ Foot Section for Semi & Full Electric Beds, Junction Boxes, Product Usage: The Invacare Bariatric home ca
Recalled August 17, 2016 · FDA recall Z-2401-2016 · Invacare
Hazard
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. · FDA Class II
Units
3,050 units
Sold at
US Nationwide Distribution including DC and PR. Internationally Canada.
Description
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.
Product
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.
Manufacturer(s)
Invacare Corporation
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →