CME America, LLC recalls CMExpress Microbore Set, REF: A120-160C
Recalled Product
CMExpress Microbore Set, REF: A120-160C
Hazard / Issue
Infusion administration sets may have a delivery inaccuracy over plus/minus 13%, ranging from minus 42.8% to plus 17.5%. Use of the infusion pump system could cause over-infusion or under-infusion of therapy
Issued by
FDA
Affected States: CA, IN, LA, MO, FL, IL, ME, MN, CO, VA, OK, NE, GA, AL, KY, IA, MS, ID, TX, SC, OH, SD, NV, MI, WY, NC, PA, TN, KS, NJ, OR, AR, NM, MA, NY, DC, RI, MD, WA, WI, AZ, NH, UT, HI, AK, MT, ND, VT, CT
Lot/Code Info: All lots within expiry
View official government recall
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