Food Recall Check
Class I · High risk Terminated Initiated Feb 1, 2013 (14 years ago)

GoldCoast Salads Blue Crab Spread recall

Recalled by GoldCoast Salads · Naples, FL, United States

Class I — High risk. Reasonable probability of serious harm or death.

Why it was recalled

Product may be contaminated with Listeria Monocytogenes

Pathogen: Listeria

Listeria monocytogenes can grow even in the fridge and is especially dangerous in pregnancy.

The most serious food recalls: a contaminated product can cause outbreaks, hospitalisations and deaths, especially for pregnant people, young children, older adults and anyone with a weakened immune system. All bacteria & viruses recalls.

What was recalled

GoldCoast Salads Blue Crab Spread (8oz and 16oz in flexible plastic cup with flexible plastic lids - keep refrigerate at 38 or below)

Quantity: 6,857 cases total

Food: Seafood & fish

Lot codes, dates and UPCs

A recall covers only these codes. Compare them with the lot number, best-by date or UPC printed on your package.

8oz = UPC Code = 33555 00325 exp 01/31/2013 and exp 02/14/2013B 16oz = UPC Code 33555 00125 exp 01/31/2013 and exp 02/14/2013B

Where it was sold

Alabama Florida Georgia Massachusetts Maryland North Carolina New Jersey New York Pennsylvania Tennessee Virginia

FDA's distribution note: AL, FL, GA, MA, MD, NC, NJ, NY, PA, TN and VA

Do not eat it. Class I means FDA judged there is a reasonable probability of serious illness or death. If the brand, size and lot or date code on your package match, throw the product away or return it to the store for a refund, and clean any surface or container it touched. If anyone has eaten it and feels unwell, contact a doctor and mention the recall. FDA lists this recall as terminated: the company has finished removing the product, so it should no longer be on shelves - but it can still be in a freezer or pantry.

Recalling firm
GoldCoast Salads
Initiated by
Voluntary: Firm initiated
Recall initiated
Feb 1, 2013
In FDA report of
Mar 6, 2013
Terminated
Aug 11, 2014
FDA recall number
F-1032-2013 · event 64292
Official record
FDA enforcement report search

Also recalled with it (3 more products)

FDA files each product of one recall action separately; these share the same FDA event.

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