Food Recall Check
Class II · Moderate risk Terminated Initiated Sep 2, 2014 (12 years ago)

Tullia's Italian Meatless Pasta Sauce recall

Recalled by Tullia's · Spokane, WA, United States

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

Why it was recalled

Italian Meatless Pasta Sauce is recalled because review of the production records revealed that one batch of sauce produced had a pH high enough to allow the growth of Clostridium botulinum, a bacterium which can cause life-threatening illness or death.

Pathogen: Botulism

Clostridium botulinum toxin, a risk in improperly canned or under-processed foods.

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

Tullia's Italian Meatless Pasta Sauce, packaged in a 16 oz. (436g) and 32 oz. (872g) glass jars with one-piece metal closures. The 32 oz. (872g) glass jar has the UPC 7 48863 64322 3. The 16 oz (436g) glass jar has the UPC 7 48863 64321 6.

Quantity: 312 jars (16 oz. each) and 172 jars (32 oz. each)

Food: Pasta, rice & grains 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.

Code 530140

Where it was sold

Washington

FDA's distribution note: distributed in Spokane area of Washington.

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. 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
Tullia's
Initiated by
Voluntary: Firm initiated
Recall initiated
Sep 2, 2014
In FDA report of
Oct 22, 2014
Terminated
Feb 13, 2015
FDA recall number
F-0024-2015 · event 69168
Official record
FDA enforcement report search

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