CLASS I Food recall · Reported 16 Jan 2013 · FDA Enforcement Report

Product labeled in part: ***Paramount Reserve*** recalled

Multiexport Foods is recalling Product labeled in part: ***Paramount Reserve***, distributed in 43 states. The recall was initiated on 18 Dec 2012 and the FDA has classified it as Class I.

Check your package

Lot, batch or date codesTwin Pack 12 oz = 931-59733-2, 933-59753-1, 933-59754-2, 875-701413-1, and 890-701413-1 // 12oz UPC 6 88264 86705 0 ===================================== 1.25 lb Pack = 870-701342-1, 873-701342-1, 870-701344-1, 873-701360-1, 870-701364-1, 873-701364-1, 900-701344-1, 873-701344-1, 873-701360-1, 886-701413-1, 900-701413-1, 873-701344-1, and 870-701360-1 // 1.25 lb UPC 6 88264 86664 0

Do not eat it. Return it to the store for a refund or throw it away. If you have symptoms after eating it, contact a doctor.

Recall details

Recall number
F-0875-2013
FDA event ID
63980
Recalling firm
Multiexport Foods, Miami, FL
Classification
Class I
Status
Terminated
Recall initiated
18 Dec 2012
FDA classified
8 Jan 2013
Reported
16 Jan 2013
Type
Voluntary: Firm initiated
Customers notified by
Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit
Reason category
Listeria
Product category
Salmon

Timeline

18 Dec 2012Recall initiated by company
8 Jan 2013Classified by FDA+21 days
16 Jan 2013Published in enforcement report+8 days

Companies usually start a recall weeks before the FDA classifies and publishes it; the gap above is that lag.

Reason for recall

The firm initiated the recall based on positive results for Listeria monocytogenes obtained from a composite sample tested by a private laboratory.

Listeria monocytogenes can grow at refrigerator temperatures. Infection is most dangerous for pregnant women, newborns, older adults and people with weakened immune systems. Symptoms can appear up to 70 days after eating contaminated food.

Product as listed by the FDA

Product labeled in part: ***PARAMOUNT RESERVE***PRODUCT OF CHILE FARM RAISED ATLANTIC SALMON PACKED BY: ALIMENTOS MULTIEXPORT S.A. *** DISTRIBUTED BY MULTIEXPORT FOODS INC. 703 WATERFORD WAY (NW 62ND AVE) SUITE 510, MIAMI, FL 33126***

Where it was distributed

Alabama, Arkansas, Alaska, Arizona, California, Colorado, Connecticut, Delaware, Florida, Georgia, Hawaii, Iowa, Idaho, Illinois, Indiana, Kansas, Kentucky, Louisiana, Massachusetts, Maryland, Maine, Montana, Missouri, Mississippi, Nebraska, North Carolina, New Hampshire, New Jersey, New York, New Mexico, Nevada, Ohio, Oklahoma, Pennsylvania, Puerto Rico, South Carolina, Tennessee, Texas, Utah, Washington, Virginia, Wisconsin and West Virginia

AlaskaAlabamaArkansasArizonaCaliforniaColoradoConnecticutDelawareFloridaGeorgiaHawaiiIowaIdahoIllinoisIndianaKansasKentuckyLouisianaMassachusettsMaryland

Questions about this recall

Why was it recalled?

The firm initiated the recall based on positive results for Listeria monocytogenes obtained from a composite sample tested by a private laboratory.

Which lots are affected?

Twin Pack 12 oz = 931-59733-2, 933-59753-1, 933-59754-2, 875-701413-1, and 890-701413-1 // 12oz UPC 6 88264 86705 0 ===================================== 1.25 lb Pack = 870-701342-1, 873-701342-1, 870-701344-1, 873-701360-1, 870-701364-1, 873-701364-1, 900-701344-1, 873-701344-1, 873-701360-1, 886-701413-1, 900-701413-1, 873-701344-1, and 870-701360-1 // 1.25 lb UPC 6 88264 86664 0

Where was it sold?

Alabama, Arkansas, Alaska, Arizona, California, Colorado, Connecticut, Delaware, Florida, Georgia, Hawaii, Iowa, Idaho, Illinois, Indiana, Kansas, Kentucky, Louisiana, Massachusetts, Maryland, Maine, Montana, Missouri, Mississippi, Nebraska, North Carolina, New Hampshire, New Jersey, New York, New Mexico, Nevada, Ohio, Oklahoma, Pennsylvania, Puerto Rico, South Carolina, Tennessee, Texas, Utah, Washington, Virginia, Wisconsin and West Virginia

What should I do if I have it?

Do not eat it. Return it to the store for a refund or throw it away. If you have symptoms after eating it, contact a doctor.

What does Class I mean?

Class I is the most serious FDA recall category: there is a reasonable probability that using the product will cause serious health consequences or death.

Read the official FDA notice · Source record retrieved 26 Sep 2026. The FDA describes openFDA data as unvalidated; the official notice takes precedence. This page reports the record and gives no medical advice.

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