CHAPTER IIIMRLS APPLICABLE TO PRODUCTS OF PLANT AND ANIMAL ORIGIN
F1Article 18Compliance with MRLs
F21.
A product listed in Part 1 of the MRLs register in relation to a constituent territory must not contain, from the time it is placed on the market as food or feed, or fed to animals in that constituent territory, any pesticide residue exceeding—
(a)
the MRL for that product listed in Part 2 or 3 of the MRLs register in relation to that constituent territory;
(b)
the level described in paragraphs 1A or 1B, where there is no MRL.
(1A.
Where there is no MRL for a product listed in Part 2 or 3 of the MRLs register in relation to a constituent territory, the level is the default value for an active substance as listed in Part 5 of the MRLs register in relation to that constituent territory (see Article 18A).
(1B.
Where in relation to a constituent territory—
(a)
there is no MRL for the product in Part 2 or 3 of the MRLs register,
(b)
there is no default value for an active substance listed in Part 5 of the MRLs register, and
(c)
the active substance is not listed in Part 4 of the MRLs register,
the level applicable is 0.01mg/kg.
2.
F3A competent authority may not prohibit or impede the placing on the market or the feeding to food-producing animals within F4its constituent territory of the products F5listed in Part 1 of the MRLs register in relation to its constituent territory on the grounds that they contain pesticide residues provided that:
(a)
such products comply with paragraph 1 and Article 20; or
(b)
the active substance is listed in F6Part 4 of the MRLs register in relation to that constituent territory.
3.
F7By way of derogation from paragraph 1, a competent authority may authorise, further to a post-harvest treatment with a fumigant on its constituent territory, residue levels for an active substance which exceed the limits specified in Part 2 or 3 of the MRLs register in relation to that constituent territory where the active substance/product combinations are listed in Part 7 of the MRLs register in relation to that constituent territory, provided that—
(a)
such products are not intended for immediate consumption;
(b)
appropriate controls are in place to ensure that such products cannot be made available to the end user or consumer, if they are supplied directly to the latter, until the residues no longer exceed the maximum levels specified in F8Part 2 or 3 of the MRLs register;
(c)
the other F9competent authorities have been informed of the measures taken.
F10...
F11(3A.
A competent authority may, in relation to its constituent territory—
(a)
define combinations of active substances and products for the purposes of paragraph 3;
(b)
modify or withdraw any such combinations.
(3B.
As soon as reasonably practicable after defining, modifying or withdrawing a combination in accordance with paragraph 3A the competent authority must—
(a)
notify the other competent authorities of the defining, modifying or withdrawing of the combination and the reason for that decision, and
(b)
update the MRLs register accordingly.
4.
F17(5.
Where a competent authority grants an authorisation in accordance with paragraph 4, the competent authority must—
(a)
notify the other competent authorities of that authorisation;
(b)
as soon as reasonably practicable, undertake an appropriate risk assessment with a view to setting a temporary MRL for a specified period, or taking any other necessary measure in relation to the products to which the authorisation relates.
(6.
After the completion of the risk assessment described in paragraph 5(b) the competent authority may set a temporary MRL, and Article 15(3) to (9) applies to any temporary MRL set.
(7.
In paragraph 4, “EU-derived domestic legislation” has the meaning given by section 2(2) of the European Union (Withdrawal) Act 2018.