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Ortho8, Inc. recalls EVEXIA LUXE DVT PREVENTION DEVICE, Aid in the Prevention of Deep Vein Thrombosis, REF(s): EVE-11/EVE-X11, Rx Only, Not S
Recalled August 25, 2021 · FDA recall Z-2325-2021 · Ortho8
Hazard
EVEXIA LUXE DVT PREVENTION DEVICE is marketed without FDA clearance · FDA Class II
Units
N/A
Sold at
US Nationwide distribution in the states of Al, AZ, CA, CO, CT, FL, GA, ID, IL, IN, KS, KY, LA, MD, MA, MI, MO, NC, NV, NJ, NY, OK, PA, SC, TN, TX, UT, VA.
Description
EVEXIA LUXE DVT PREVENTION DEVICE is marketed without FDA clearance
Product
EVEXIA LUXE DVT PREVENTION DEVICE, Aid in the Prevention of Deep Vein Thrombosis, REF(s): EVE-11/EVE-X11, Rx Only, Not Sterile
Manufacturer(s)
Ortho8, Inc.
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →