GE Healthcare, LLC recalls MAC VU360, Electrocardiograph
Recalled Product
MAC VU360, Electrocardiograph
Hazard / Issue
Incorrect patient identification and/or patient demographic errors.
Issued by
FDA
Affected States: AL, AR, AZ, CA, CO, CT, DC, DE, FL, GA, HI, IA, ID, IL, IN, KS, KY, LA, MA, MD, ME, MI, MN, MO, MS, MT, NC, NE, NH, NJ, NM, NV, NY, OH, OK, OR, PA, RI, SC, SD, TN, TX, UT, VA, VT, WA, WI, WV, WY
Lot/Code Info: Model: 2030360 001
View official government recall
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