RecallHawk
Class I Recall

Tone s Taco Seasoning Blend, Plastic Bottles / 12 bottles per case with best by dates of SEPT 03 24 and SEPT 06 24, d

B&G Foods North America, Inc

Summary

The FDA issued a Class I for Tone s Taco Seasoning Blend, Plastic Bottles / 12 bottles per case with best b by B&G Foods North America, Inc. Reason: Product was recalled due to the presence of undeclared wheat..

Details

Source

Food Recall

External ID

F-0018-2022

Action Date

2021-10-20

Status

Terminated

Category

food

Product Description

Tone s Taco Seasoning Blend, Plastic Bottles / 12 bottles per case with best by dates of SEPT 03 24 and SEPT 06 24, due to the

Lot/Code Info: Best By SEP 03 24 Best By SEP 06 24

Quantity Affected: 3,867 cases of 23 oz.

Reason for Recall

Product was recalled due to the presence of undeclared wheat.

Distribution

The product was distributed in the United States to the following States: AL, AR, AZ, CA, CO, CT, DE, FL, GA, HI, IA, ID, IL, IN, KS, KY, LA, MD, ME, MI, MN, MO, MS, MT, NC, ND, NE, NH, NJ, NM, NV, NY, OH, OK, PA, SC, TN, SD, TX, UT, VA, WI, WV, WY .

Type: Voluntary: Firm initiated

Recall Initiated: 2021-09-29

Company

Context & Analysis

This is a Class I recall. Class I recalls are the most serious — there is a reasonable probability that use of or exposure to the product will cause serious health consequences or death.

This was one of 17 food recalls issued in the same week, part of 204 food-related FDA actions this month.

B&G Foods North America, Inc has 3 FDA actions in our database, including 3 recalls.

Frequently Asked Questions

What is a Class I recall?

A Class I recall is the most serious type. The FDA has determined there is a reasonable probability that the product will cause serious adverse health consequences or death. Consumers should stop using the product immediately.

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 (B&G Foods North America, Inc) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.

How often does B&G Foods North America, Inc have FDA actions?

B&G Foods North America, Inc has 3 FDA actions in our database, including 3 recalls and 0 device clearances.

Where can I find the official FDA record?

The official record is available on FDA.gov. Search for "F-0018-2022" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.

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