Food Recall Check
Class I · High risk Terminated Initiated Jan 19, 2024 (3 years ago)

Al Amir Fresh Foods Harissa Spicy Hummus With a Kick recall

Recalled by Lydia Pack 3 Inc · Milwaukie, OR, United States

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

Why it was recalled

Hummus product label declares Tahini but does not declare sesame.

A label that does not match the product can hide an ingredient someone must avoid, or show a wrong use-by date. All labeling errors recalls.

What was recalled

Al Amir Fresh Foods Harissa Spicy Hummus With a Kick, packaged in round plastic clear container, net wt. 8oz. There are 12 containers per case. UPC on 8oz container: 7 55134 12352 0. The recalled product label declares: Ingredients: Garbanzo Beans, Tahini Paste, Garlico (Fresh Garlic/Oil/Lemon/Salt), Hot Chili Peppers, Natural Citric Acid, Salt.

Quantity: 3,000 to 4,000 packages for each product

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.

All dates up to and includes 1/25/2024

Where it was sold

Oregon Washington

FDA's distribution note: Distributed in OR and WA.

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
Lydia Pack 3 Inc
Initiated by
Voluntary: Firm initiated
Recall initiated
Jan 19, 2024
In FDA report of
Feb 21, 2024
Terminated
Apr 16, 2024
FDA recall number
F-0868-2024 · event 93850
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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