RecallHawk
Class II Recall

Member's Mark brand Roasted Red Pepper Hummus; 32 oz (907 g) Plastic Container with UPC# 193968044268

Cedar's Mediterranean Foods, Inc.

Summary

The FDA issued a Class II for Member's Mark brand Roasted Red Pepper Hummus; 32 oz (907 g) Plastic Container w by Cedar's Mediterranean Foods, Inc.. Reason: Potential presence of foreign objects..

Details

Source

Food Recall

External ID

F-0243-2025

Action Date

2024-12-11

Status

Terminated

Category

food

Product Description

Member's Mark brand Roasted Red Pepper Hummus; 32 oz (907 g) Plastic Container with UPC# 193968044268

Lot/Code Info: Best if used by Nov 21, 2024 (20I24) & Nov 23, 2024 (40I24)

Quantity Affected: 23,136 units

Reason for Recall

Potential presence of foreign objects.

Distribution

NC, TX, OH, NY, GA, MN, IN, VA, MD, LA

Type: Voluntary: Firm initiated

Recall Initiated: 2024-10-09

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

Cedar's Mediterranean Foods, Inc. has 2 FDA actions in our database, including 2 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 (Cedar's Mediterranean Foods, Inc.) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.

How often does Cedar's Mediterranean Foods, Inc. have FDA actions?

Cedar's Mediterranean Foods, Inc. has 2 FDA actions in our database, including 2 recalls and 0 device clearances.

Where can I find the official FDA record?

The official record is available on FDA.gov. Search for "F-0243-2025" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.

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