RecallHawk
Class III Recall

Priyems Sambar Spicy Lentil Soup 800 grams (1.76 lbs) UPC 8 61754 00010 0, 8 retail units per wholesale case, Frozen

Yem Foods LLC

Summary

The FDA issued a Class III for Priyems Sambar Spicy Lentil Soup 800 grams (1.76 lbs) UPC 8 61754 00010 0, 8 ret by Yem Foods LLC. Reason: undeclared wheat starch sub-ingredient found in the asafoetida used in the products.

Details

Source

Food Recall

External ID

F-1678-2022

Action Date

2022-09-07

Status

Terminated

Category

food

Product Description

Priyems Sambar Spicy Lentil Soup 800 grams (1.76 lbs) UPC 8 61754 00010 0, 8 retail units per wholesale case, Frozen

Lot/Code Info: All products with Use By Date 08/08/23 or earlier

Quantity Affected: 2313 cases

Reason for Recall

undeclared wheat starch sub-ingredient found in the asafoetida used in the products

Distribution

CT, DE, IL, IN, KY, MA, MI, NC, NH, NJ, NY, OH, PA, TN, WI

Type: Voluntary: Firm initiated

Recall Initiated: 2022-08-08

Company

Yem Foods LLC

Wixom, MI

Context & Analysis

This is a Class III recall. Class III recalls involve products unlikely to cause adverse health consequences, but that violate FDA regulations.

This was one of 111 food recalls issued in the same week, part of 204 food-related FDA actions this month.

Yem Foods LLC has 4 FDA actions in our database, including 4 recalls.

Frequently Asked Questions

What is a Class III recall?

A Class III recall involves products that are unlikely to cause adverse health effects but violate FDA labeling or manufacturing regulations.

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 (Yem Foods LLC) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.

How often does Yem Foods LLC have FDA actions?

Yem Foods LLC has 4 FDA actions in our database, including 4 recalls and 0 device clearances.

Where can I find the official FDA record?

The official record is available on FDA.gov. Search for "F-1678-2022" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.

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