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Compass Health Brands (Corporate Office) recalls MediPress pneumatic compression system, Half Leg-Segmental Gradient, Model #6102-S
Recalled May 22, 2019 · FDA recall Z-1343-2019 · Compass Health Brands (Corporate Office)
Hazard
Product design change did not receive proper premarket clearance and lacks a 510 (k) · FDA Class II
Sold at
Domestically to AL, AR, AZ, CA, CO, FL, GA, IA, IL, IN, KS, KY, LA, MA, MD, MI, MO, MS, MT, NC, NE, NJ, NV, NY, OH, OK, OR, PA, SC, TN, TN, KY, TX, UT, VA, WA, WI & WY Internationally to Canada
Description
Product design change did not receive proper premarket clearance and lacks a 510 (k)
Product
MediPress pneumatic compression system, Half Leg-Segmental Gradient, Model #6102-S
Manufacturer(s)
Compass Health Brands (Corporate Office)
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →