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Invacare Corporation recalls Foot Section - BAR5490IVC
Recalled February 15, 2017 · FDA recall Z-1184-2017 · Invacare
Hazard
A quality issue with the junction box used in the bariatric bed junction that may omit sparks and result into a fire. · FDA Class II
Units
292 units
Sold at
Products were distributed in the following states: AK, AL, AR, CA, CO, CT, FL, HI, ID, IL, IN, KS, LA, MA, MD, ME, MI, MN, MO, MS, NC, NJ, NM, NY, OH, OK, OR, PA, RI, SC, SD, TN, TX, UT, VA, WA, and WI. No foreign accounts
Description
A quality issue with the junction box used in the bariatric bed junction that may omit sparks and result into a fire.
Product
Foot Section - BAR5490IVC
Manufacturer(s)
Invacare Corporation
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →