Food Recall Check
Class II · Moderate risk Terminated Initiated Feb 12, 2021 (6 years ago)

Brite Harbor Caesar Dressing & Dip recall

Recalled by Litehouse Inc · Sandpoint, ID, United States

Class II — Moderate risk. May cause temporary or reversible harm; serious harm unlikely.

Why it was recalled

Undeclared anchovies

Undeclared allergen: Fish

For someone with a food allergy the label is the only protection. An undeclared allergen can trigger a severe reaction even in a trace amount, which is why most of these recalls are Class I. All undeclared allergens recalls.

What was recalled

Brite Harbor Caesar Dressing & Dip, 1.5 oz pillows (pouches), item # 16002. The front label states "***BRITE HARBOR CAESAR DRESSING & DIP***" and the back label states "***BLUE CHEESE DRESSING***CONTAINS Egg, Milk ***".

Quantity: 225 cases (60/1.5 oz. pouches per case)

Food: Sauces, dips & dressings

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.

lot code on pillows (pouches): 03 071321 16002. lot code on master case: 16002 03 07/13/21 NON-REF 03 = facility code Hurricane Utah 071321 = best if used by date July 13, 2021

Where it was sold

Arizona California Idaho Michigan Oregon Washington Wisconsin

FDA's distribution note: Distributed in AZ, CA, ID, MI, OR, WA and WI.

Check the codes, then return or discard. Class II means eating it may cause temporary or reversible health problems. If your package matches the recalled codes, do not eat it - return it to the store or throw it away. The risk from an undeclared allergen is to people allergic to fish; for anyone else the product is generally not a safety concern. 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
Litehouse Inc
Initiated by
Voluntary: Firm initiated
Recall initiated
Feb 12, 2021
In FDA report of
Mar 3, 2021
Terminated
Mar 22, 2021
FDA recall number
F-0324-2021 · event 87335
Official record
FDA enforcement report search

Other recalls by Litehouse Inc

Class I · High risk Terminated Undeclared egg

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Litehouse Inc 7 states F-3514-2017

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