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Document 02010D0381-20161006
Commission Decision of 8 July 2010 on emergency measures applicable to consignments of aquaculture products imported from India and intended for human consumption (notified under document C(2010) 4563) (Text with EEA relevance) (2010/381/EU)
Consolidated text: Commission Decision of 8 July 2010 on emergency measures applicable to consignments of aquaculture products imported from India and intended for human consumption (notified under document C(2010) 4563) (Text with EEA relevance) (2010/381/EU)
Commission Decision of 8 July 2010 on emergency measures applicable to consignments of aquaculture products imported from India and intended for human consumption (notified under document C(2010) 4563) (Text with EEA relevance) (2010/381/EU)
02010D0381 — EN — 06.10.2016 — 002.001
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COMMISSION DECISION of 8 July 2010 on emergency measures applicable to consignments of aquaculture products imported from India and intended for human consumption (notified under document C(2010) 4563) (Text with EEA relevance) (OJ L 174 9.7.2010, p. 51) |
Amended by:
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Official Journal |
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No |
page |
date |
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L 308 |
21 |
8.11.2012 |
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COMMISSION IMPLEMENTING DECISION (EU) 2016/1774 of 4 October 2016 |
L 271 |
7 |
6.10.2016 |
COMMISSION DECISION
of 8 July 2010
on emergency measures applicable to consignments of aquaculture products imported from India and intended for human consumption
(notified under document C(2010) 4563)
(Text with EEA relevance)
(2010/381/EU)
Article 1
This Decision shall apply to the importation of consignments of aquaculture products from India intended for human consumption (‘consignments’).
Article 2
The analytical test must have been carried out on an official sample, in particular with a view to detecting the presence of chloramphenicol, tetracycline, oxytetracycline and chlortetracycline and of metabolites of nitrofurans.
Those samples must have been analysed using analytical methods in conformity with Articles 3 and 4 of Decision 2002/657/EC.
Article 3
Article 4
The consignments from which official samples have been taken pursuant to Articles 2(2) and 3(1) shall be kept under official detention by the competent authority of the Member State concerned, until the analytical tests have been completed.
Those consignments may be placed on the market only if the results of the analytical tests confirm that they comply with Regulation (EC) No 470/2009.
Article 5
Member States shall immediately inform the Commission of the results of the analytical tests if those tests reveal the presence of residues of any pharmacologically active substance:
classified in accordance with Article 14(2)(a), (b) or (c) of Regulation (EC) No 470/2009 at a level exceeding the maximum residue limit established pursuant to that Regulation; or
not classified in accordance with Article 14(2)(a), (b) or (c) of Regulation (EC) No 470/2009; however, the Member State concerned is not required to immediately inform the Commission of the results of such tests where the level of residues is lower than:
the reference point for action established for that substance pursuant to Regulation (EC) No 470/2009; or
the minimum required performance limit established for that substance pursuant to Decision 2002/657/EC.
The results of those analytical tests shall be notified to the Commission under the rapid alert system established pursuant to Article 50 of Regulation (EC) No 178/2002.
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Article 6
All expenditure incurred in the application of this Decision shall be charged to the consignor, the consignee or the agent of either the consignor or the consignee.
Article 7
Decision 2009/727/EC is repealed.
Article 8
This Decision is addressed to the Member States.