Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
MAC VU360 Recalled by GE Healthcare, LLC Due to Incorrect patient identification and/or patient demographic errors.
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 GE Healthcare, LLC directly.
Affected Products
MAC VU360, Electrocardiograph
Quantity: 5,284 units
Why Was This Recalled?
Incorrect patient identification and/or patient demographic errors.
Where Was This Sold?
This product was distributed to 49 states: AL, AZ, AR, CA, CO, CT, DE, FL, GA, HI, ID, IL, IN, IA, KS, KY, LA, ME, MD, MA, MI, MN, MS, MO, MT, NE, NV, NH, NJ, NM, NY, NC, OH, OK, OR, PA, RI, SC, SD, TN, TX, UT, VT, VA, WA, WV, WI, WY, DC
About GE Healthcare, LLC
GE Healthcare, LLC has 474 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report