Food Recall Check
Class I · High risk Terminated Initiated Aug 25, 2014 (12 years ago)

Basil Pesto Pasta packaged in a non-flex plastic tub recall

Recalled by TJs Place · Kirkland, WA, United States

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

Why it was recalled

Tj's Place is recalling Basil Pesto Pasta packed in 8 oz. plastic tubs because it has the potential to 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

Basil Pesto Pasta packaged in a non-flex plastic tub, net wt 8 oz. A green sticker is placed on the lid of the package which contains the lot code. Product is refrigerated

Quantity: 20-40 units

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.

0825, 0826, 0827, and 0828. Code represents month (08) and day (25) of expiration

Where it was sold

Washington

FDA's distribution note: Washington State

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
TJs Place
Initiated by
Voluntary: Firm initiated
Recall initiated
Aug 25, 2014
In FDA report of
Oct 8, 2014
Terminated
Nov 14, 2014
FDA recall number
F-2539-2014 · event 69151
Official record
FDA enforcement report search

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