Haw. Rev. Stat. § 328-17.5: Principal labeler responsibility under recall of drug.
Where this section sits in the code
- HI Code
- Division 1
- Title 19
- Chapter 328
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.
Collected 2026-09-14T18:32:11Z. Source file · JSON