Food Recall Check
Class II · Moderate risk Terminated Initiated Aug 6, 2018 (8 years ago)

Summer squash noodles packaged under the following brands recall

Recalled by Banks Square Market Corp dba The Produce Connection · Wakefield, MA, United States

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

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

Summer squash noodles packaged under the following brands - the PICK UPC: 8 54340 00706 5

Quantity: 2,727 cases (total for all products)

Food: Pasta, rice & grains

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 lots within expiry.

Where it was sold

Massachusetts Maryland New York

FDA's distribution note: Product was directly distributed to the following states: MA, MD, NY

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
Banks Square Market Corp dba The Produce Connection
Initiated by
Voluntary: Firm initiated
Recall initiated
Aug 6, 2018
In FDA report of
Aug 29, 2018
Terminated
Sep 27, 2018
FDA recall number
F-1959-2018 · event 80732
Official record
FDA enforcement report search

Also recalled with it (2 more products)

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

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