Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
MediPress pneumatic compression system Full Leg (Medium)-Segmental Gradient Recalled by Compass Health Brands (Corporate Office) Due to Product design change did not receive proper premarket...
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 Compass Health Brands (Corporate Office) directly.
Affected Products
MediPress pneumatic compression system Full Leg (Medium)-Segmental Gradient, Model #6103M-S
Why Was This Recalled?
Product design change did not receive proper premarket clearance and lacks a 510 (k)
Where Was This Sold?
This product was distributed to 36 states: AL, AZ, AR, CA, CO, FL, GA, IL, IN, IA, KS, KY, LA, MD, MA, MI, MS, MO, MT, NE, NV, NJ, NY, NC, OH, OK, OR, PA, SC, TN, TX, UT, VA, WA, WI, WY
About Compass Health Brands (Corporate Office)
Compass Health Brands (Corporate Office) has 9 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report