RecallHawk
Class II Recall

Ivar's Kettle Classic Clam Chowder With Uncured Bacon, Item #1952, Costco Item #1270666. The soup is refrigerated and p

Ivar's Commissary

Summary

The FDA issued a Class II for Ivar's Kettle Classic Clam Chowder With Uncured Bacon, Item #1952, Costco Item # by Ivar's Commissary. Reason: Plastic fragments..

Details

Source

Food Recall

External ID

F-0159-2022

Action Date

2021-11-10

Status

Terminated

Category

food

Product Description

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***".

Lot/Code Info: Use By Date: 12-22-2021

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

Reason for Recall

Plastic fragments.

Distribution

distributed in Illinois, Indiana, Iowa, Kansas, Kentucky, Michigan, Minnesota, Missouri, Nebraska, North Dakota, Ohio, South Dakota, and Wisconsin.

Type: Voluntary: Firm initiated

Recall Initiated: 2021-10-18

Company

Ivar's Commissary

Mukilteo, WA

Context & Analysis

This is a Class II recall. Class II recalls indicate that use of or exposure to the product may cause temporary or medically reversible health consequences, or that the probability of serious consequences is remote.

This was one of 54 food recalls issued in the same week, part of 204 food-related FDA actions this month.

Frequently Asked Questions

What is a Class II recall?

A Class II recall means the product may cause temporary or medically reversible adverse health consequences, or the probability of serious adverse consequences is remote. Consumers should discontinue use.

What should I do if I have this product?

Stop using the product. Check the product against the specific lot numbers or identifiers listed in the recall. Contact the manufacturer (Ivar's Commissary) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.

How often does Ivar's Commissary have FDA actions?

This is the only FDA action we have on record for Ivar's Commissary in our database.

Where can I find the official FDA record?

The official record is available on FDA.gov. Search for "F-0159-2022" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.

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