United States Food and Drug AdministrationNew York District OfficeNotice of FDA ActionEntry Number:ANJ-OO18000-7Notice Number:2May 7,2015Importer:W & T Seafood Corp.50 Franklin AveBrooklyn, NY11205-1504><Port of Entry:4601, Newark, NJCarrier:ORIENT OVERSEAS CONTAINER LIN;Date Received:April 30, 2015Arrival Date:May 1,2015Filer of Record:RICHARD H. YING C.H.B., Jamaica, NY11434-5463Consignee:W & T Seafood Corp., Brooklyn, NY11205-1504HOLD DESJGNATEDSummary of Current Status of Individual LinesLine ACSIFDA Product Description Quantity Current Status001/001 FROZEN TILAPIA WHOLE ROUND 19958 KG Detained 05-06-2015* = Status change since the previous notice. Read carefully the sections which follow for important information regarding these lines.@ = Consignee 10FDA will not request redelivery for examination or sampling, if the products not released by FDA are moved, following USCS conditional release to a location within the metropolitan area or to a location approved by the FDA office at the number below.All products in this entry not listed above may proceed without FDA examination. This notice does not constitute assurance the products involved comply with provisions of the Food, Drug, and Cosmetic Act or other related acts, and does not preclude action should the products later be found violative.DETENTION WITHOUT EXAMINATIONThe following products are subject to refusal pursuant to the Federal Food Drug and Cosmetic Act (FD&CA), Public Health Service Act (PHSA),or other related acts in that they appear to be adulterated, misbranded or otherwise in violation as indicated below:Line ACSIFDA Product Description Respond ByNotice of FDA Action Entry Number: ANJ-0018000-7Notice Number 2 Page: 2001/001 FROZEN TILAPIA WHOLE ROUND FD&CA Section 402(a)(1), 801(a)(3); ADULTERATIONMay 27, 2015The article appears to contain Salmonella, a poisonous and deleterious substance which may render itinjurious to health. See FDA Import Alert No. 16-81 (WWW.FDA.GOV). You may submit evidence that theproduct is in compliance, such as a private lab analysis. Please send responsive documents to ITACS. Toaccess ITACS directly: https://itacs.fda.govFD&CA Section 402(a)(2)(C)(ii); 801 (a)(3); ADULTERATION The article appears to contain a new animal drug (or conversion product thereof) that is unsafe within the meaning of section 512. Product contains gentian violet. See FDA Import Alert No. 16-124 (WWW.FDA.GOV).Youmaysubmitevidencethatproductisincompliance(e.g.. private lab analysis). Please send responsive documents to ITACS. To access ITACS directly: https://itacsfda.govPlease direct your response to:(718) 662-5477Herman B. Janiger, Compliance Officer(718) 662-5662 (FAX)(Region/District)HERMAN.JANIGER@FDA.HHS.GOVUS Food and Drug Administration158-15 Liberty AvenueJamaica, NY 11433You have the right to provide oral or written testimony, to the Food & Drug Administration, regarding the admissibility of the article(s) or the manner in which the article(s) can be brought into compliance. This testimony must be provided to FDA on or before the dates shown above.Notice Prepared For: The District Director, US. Food and Drug Administration Notice Prepared By: FS
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