Food Recall Check
Class II · Moderate risk Terminated Initiated Oct 18, 2021 (5 years ago)

Ivar's Kettle Classic Clam Chowder With Uncured Bacon recall

Recalled by Ivar's Commissary · Mukilteo, WA, United States

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

Why it was recalled

Plastic fragments.

Hard or sharp fragments can cut the mouth or throat, break teeth or cause choking. They usually come from equipment wear or packaging on the production line. All foreign material recalls.

What was recalled

Ivar's Kettle Classic Clam Chowder With Uncured Bacon, Item #1952, Costco Item #1270666. The soup is refrigerated and packaged in 24 oz. clear plastic cups, in a double pack surrounded by a printed paperboard sleeve (2/24 cups per sleeve). Retail package's UPC 0 30383 19649 6. There are 8 sleeves per master case. Master case label is read in part: "***Ivar's #1952 ALL NATURAL WHITE CLAM CHOWDER *** PERISHABLE KEEP REFIGERATED *** EIGHT [2 X 24 OZ PACKAGES] *** NET WT. 24 LB***".

Quantity: 1871 cases or total 14,968 sleeves (2/24 oz. cups per sleeve)

Food: Seafood & fish

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.

Use By Date: 12-22-2021

Where it was sold

Iowa Illinois Indiana Kansas Kentucky Michigan Minnesota Missouri North Dakota Nebraska Ohio South Dakota Wisconsin

FDA's distribution note: distributed in Illinois, Indiana, Iowa, Kansas, Kentucky, Michigan, Minnesota, Missouri, Nebraska, North Dakota, Ohio, South Dakota, and Wisconsin.

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
Ivar's Commissary
Initiated by
Voluntary: Firm initiated
Recall initiated
Oct 18, 2021
In FDA report of
Nov 10, 2021
Terminated
May 13, 2022
FDA recall number
F-0159-2022 · event 88882
Official record
FDA enforcement report search

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