§328-17.5  Principal labeler responsibilityunder recall of drug.  Whenever the manufacturer of a drug voluntarilyrecalls the drug or the Federal Food and Drug Administration or a court ordersthe recall of a drug, the principal labeler of the drug shall remove the drugfrom all pharmacies, prescriber offices, medical oxygen distributors,distributors of non-prescription drugs, and health care facilities. [L 1982, c122, §1(1); am L 2000, c 83, §3]