Natural Health Products Regulations
62 Every manufacturer, importer or distributor who commences a recall of a natural health product shall, within three days after the day on which the recall is commenced, provide the Minister with the following information in respect of the natural health product:
(a) the proper name and the common name of each medicinal ingredient that it contains;
(b) each brand name under which it is sold;
(c) its product number;
(d) the number of each lot or batch recalled;
(e) the name and address of the manufacturer, importer or distributor who commenced the recall;
(f) the reasons for commencing the recall;
(g) the name and address of each person to whom the recalled product was sold by the manufacturer, importer or distributor who commenced the recall;
(h) the quantity of the recalled product that was sold by the manufacturer, importer or distributor who commenced the recall;
(i) the quantity of the recalled product remaining in the possession of the manufacturer, importer or distributor who commenced the recall;
(j) if the recall was commenced by a manufacturer, the quantity of the recalled product that they manufactured;
(k) if the recall was commenced by an importer, the quantity of the recalled product that they imported and the name and address of each person that sold it to them;
(l) if the recall was commenced by a distributor, the quantity of the recalled product that was sold to them and the name and address of each person that sold it to them; and
(m) a description of any other action, in respect of the recall, that the manufacturer, importer or distributor who commenced the recall is taking.
- SOR/2022-146, s. 12
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