Z-2587-2020 Class I Terminated

Recalled by CME America, LLC — Golden, CO

Recall Details

Product Type
Devices
Report Date
July 22, 2020
Initiation Date
June 16, 2020
Termination Date
May 9, 2022
Voluntary/Mandated
Voluntary: Firm initiated
Product Quantity
1824

Product Description

CMExpress Needleless Y Site Microbore Set, REF: A120-160CYNVK

Reason for Recall

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

Distribution Pattern

U.S: 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. OUS (Foreign): Canada, UK

Code Information

All lots within expiry