RecallHawk
Class I Recall

Sheila G's Gluten Free Reese's Pieces Brownie Brittle, 4 oz bag (Retail bag UPC 711747 011562)

Kar Nut Products Company

Summary

The FDA issued a Class I for Sheila G's Gluten Free Reese's Pieces Brownie Brittle, 4 oz bag (Retail bag UPC by Kar Nut Products Company. Reason: Product is labeled "Gluten Free" but may contain undeclared wheat..

Details

Source

Food Recall

External ID

F-0738-2023

Action Date

2023-04-26

Status

Terminated

Category

food

Product Description

Sheila G's Gluten Free Reese's Pieces Brownie Brittle, 4 oz bag (Retail bag UPC 711747 011562)

Lot/Code Info: SG 1054 15/NOV/2023 1S and SG 1054 15/NOV/2023 2S

Quantity Affected: 3,944 cases

Reason for Recall

Product is labeled "Gluten Free" but may contain undeclared wheat.

Distribution

Nationwide through distributor in IL

Type: Voluntary: Firm initiated

Recall Initiated: 2023-03-23

Company

Kar Nut Products Company

Madison Heights, MI

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

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 (Kar Nut Products Company) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.

How often does Kar Nut Products Company have FDA actions?

This is the only FDA action we have on record for Kar Nut Products Company in our database.

Where can I find the official FDA record?

The official record is available on FDA.gov. Search for "F-0738-2023" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.

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