RecallHawk
Class II Recall

H-E-B Creamy Tomato Basil Soup NET WT 32 oz. packaged in a clear glass jar UPC 4122070619

Fischer & Wieser Specialty Foods, Inc.

Summary

The FDA issued a Class II for H-E-B Creamy Tomato Basil Soup NET WT 32 oz. packaged in a clear glass jar UPC 4 by Fischer & Wieser Specialty Foods, Inc.. Reason: Potential to contain glass.

Details

Source

Food Recall

External ID

F-0273-2022

Action Date

2021-12-15

Status

Terminated

Category

food

Product Description

H-E-B Creamy Tomato Basil Soup NET WT 32 oz. packaged in a clear glass jar UPC 4122070619

Lot/Code Info: Best By/Sell By: 10-14-22 Lot 22871-1 through Lot 22871-10

Quantity Affected: 4579 units

Reason for Recall

Potential to contain glass

Distribution

Texas

Type: Voluntary: Firm initiated

Recall Initiated: 2021-11-19

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 60 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 (Fischer & Wieser Specialty 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 Fischer & Wieser Specialty Foods, Inc. have FDA actions?

This is the only FDA action we have on record for Fischer & Wieser Specialty Foods, Inc. in our database.

Where can I find the official FDA record?

The official record is available on FDA.gov. Search for "F-0273-2022" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.

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