RecallHawk
Class II Recall

Meijer Sweet & Salty Trail Mix 12oz. pouch, UPC 7 08820 10371 9

Meijer Inc

Summary

The FDA issued a Class II for Meijer Sweet & Salty Trail Mix 12oz. pouch, UPC 7 08820 10371 9 by Meijer Inc. Reason: Contains undeclared ingredients including wheat and sesame.

Details

Source

Food Recall

External ID

F-0934-2023

Action Date

2023-05-31

Status

Terminated

Category

food

Product Description

Meijer Sweet & Salty Trail Mix 12oz. pouch, UPC 7 08820 10371 9

Lot/Code Info: Sell By 12/28/2023

Quantity Affected: 1,824 retail units

Reason for Recall

Contains undeclared ingredients including wheat and sesame

Distribution

IL, IN, KY, MI, MO, OH, WI

Type: Voluntary: Firm initiated

Recall Initiated: 2023-05-06

Company

Meijer Inc

Grand Rapids, MI

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

Meijer Inc has 18 FDA actions in our database, including 18 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 (Meijer Inc) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.

How often does Meijer Inc have FDA actions?

Meijer Inc has 18 FDA actions in our database, including 18 recalls and 0 device clearances.

Where can I find the official FDA record?

The official record is available on FDA.gov. Search for "F-0934-2023" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.

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