Home / Recalls / Medical Devices
Kimberly-Clark Corporation recalls Kimberly-Clark Patient Warming System - Model 1000 Control Unit The product is a thermal regulating system, indicated
Recalled December 5, 2012 · FDA recall Z-0451-2013 · Kimberly-Clark
Hazard
Error 85 alarm on the Model 1000 Control Unit was occasionally triggered inappropriately. · FDA Class II
Units
400 units
Sold at
Nationwide Distribution including AZ, AK, CA, CO, DE, DC, FL, GA. ID, IL, IN, IA, KS, KY, LA, MD, ME MA, MS, MO, MT, NE, NJ, NM, NV, NY, NC, OH, OR, PA, RI, SC, TN, TX, VA, WV, and WI
Description
Error 85 alarm on the Model 1000 Control Unit was occasionally triggered inappropriately.
Product
Kimberly-Clark Patient Warming System - Model 1000 Control Unit The product is a thermal regulating system, indicated for monitoring and controlling patient temperature.
Manufacturer(s)
Kimberly-Clark Corporation
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →