Food Recall Check
Class II · Moderate risk Terminated Initiated Oct 11, 2017 (9 years ago)

SKU 57879 Trader Joe's Organic Tomato & Roasted Red Pepper Soup recall

Recalled by Pacific Foods of Oregon, Inc. · Tualatin, OR, United States

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

Why it was recalled

Product is recalled due to potential under processing.

These are failures of the safety steps that keep food safe - cooking, pasteurising, keeping cold, sealing - even when no contaminant has yet been found. All processing & sanitation problems recalls.

What was recalled

SKU 57879, Trader Joe's Organic Tomato & Roasted Red Pepper Soup, packaged in a Tetra Pak aseptic container/carton. There are 12 cartons per case. Net Wt. 32 fl. oz. UPC 00578790. Item # 52603-05405, Pacific Organic Roasted Red Pepper and Tomato Soup Canadian, packaged in a Tetra Pak aseptic container/carton. There are 12 cartons per case. Net Wt. 32 fl. oz. No UPC.

Quantity: 160 cases or 1,920 cartons total (Trader Joe's = 10 cases (120 cartons); Pacific = 150 cases (1,800 cartons)

Food: Spices & seasonings

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.

Trader Joe's: BEST IF USED BY: 01AUG18 PFO 17213-5 Pacific (Canadian): BEST BEFORE: 01AUG18 PFO 17213-14

Where it was sold

California

FDA's distribution note: distributed in CA and in Canada.

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
Pacific Foods of Oregon, Inc.
Initiated by
Voluntary: Firm initiated
Recall initiated
Oct 11, 2017
In FDA report of
Nov 1, 2017
Terminated
Nov 15, 2017
FDA recall number
F-0031-2018 · event 78266
Official record
FDA enforcement report search

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