RecallHawk
Class II Recall

Moroccan Style Lentil Soup, 4 x 8lb pouches, Net wt. 32lb

Request Foods Incorporated

Summary

The FDA issued a Class II for Moroccan Style Lentil Soup, 4 x 8lb pouches, Net wt. 32lb by Request Foods Incorporated. Reason: Potential contamination with foreign material (wood).

Details

Source

Food Recall

External ID

F-0735-2025

Action Date

2025-04-30

Status

Terminated

Category

food

Product Description

Moroccan Style Lentil Soup, 4 x 8lb pouches, Net wt. 32lb

Lot/Code Info: Oct 11 2026 MOROCCAN STY LENTIL 19788 01115 RM 4A1 HHMM

Quantity Affected: 2094 cases

Reason for Recall

Potential contamination with foreign material (wood)

Distribution

IL, MI

Type: Voluntary: Firm initiated

Recall Initiated: 2025-04-04

Company

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 35 food recalls issued in the same week, part of 204 food-related FDA actions this month.

Request Foods Incorporated has 4 FDA actions in our database, including 4 recalls.

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

How often does Request Foods Incorporated have FDA actions?

Request Foods Incorporated 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-0735-2025" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.

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