Mako Surgical Corporation recalls RESTORIS MCK TIBIAL BASEPLATE-RM/LL used in unicompartmental
Recalled Product
RESTORIS MCK TIBIAL BASEPLATE-RM/LL used in unicompartmental knee arthroplasty and knee replacements.
Hazard / Issue
Incorrect product and/or label. Sizing is labeled incorrectly.
Issued by
FDA
Affected States: AL, AR, AZ, CA, CO, FL, GA, ID, IL, IN, KS, LA, MA, MD, MI, MN, NC, NE, NH, NJ, NY, OK, OR, PA, RI, SC, TX, UT, VA, WA, WY
Lot/Code Info: Size 2 Item # 180612 Lot # 26080317-01 and Size 7 Item # 180617 Lot # 26150217-01.
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