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§328-17.5 - Principal labeler responsibility under recall of drug.

     §328-17.5  Principal labeler responsibility under recall of drug.  Whenever the manufacturer of a drug voluntarily recalls the drug or the Federal Food and Drug Administration or a court orders the recall of a drug, the principal labeler of the drug shall remove the drug from all pharmacies, prescriber offices, medical oxygen distributors, distributors of non-prescription drugs, and health care facilities. [L 1982, c 122, §1(1); am L 2000, c 83, §3]

 

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