RecallHawk
Class I Recall

Dierbergs Kitchen Fresh Garden Spiral Pasta Salad Size: 12oz and 2 lb UPC: 231145703543 Sell By May 31, 22 Sell By Date:

Dierbergs Central Kitchen

Summary

The FDA issued a Class I for Dierbergs Kitchen Fresh Garden Spiral Pasta Salad Size: 12oz and 2 lb UPC: 23114 by Dierbergs Central Kitchen. Reason: Product Broccoli Cheddar Pasta is mislabeled as Garden Spiral Pasta and does not declare egg as an ingredient. Broccoli Cheddar Pasta has milk, egg an.

Details

Source

Food Recall

External ID

F-1131-2022

Action Date

2022-06-08

Status

Terminated

Category

food

Product Description

Dierbergs Kitchen Fresh Garden Spiral Pasta Salad Size: 12oz and 2 lb UPC: 231145703543 Sell By May 31, 22 Sell By Date: 05/31/22 Fresh Garden Spiral Pasta Salad Size: 2LB Family Pack UPC: 231145311625 Sell By Date: 05/31/22

Lot/Code Info: Sell By Date: May 31, 22

Quantity Affected: 190 lbs

Reason for Recall

Product Broccoli Cheddar Pasta is mislabeled as Garden Spiral Pasta and does not declare egg as an ingredient. Broccoli Cheddar Pasta has milk, egg and wheat allergens. Garden Spiral Pasta has milk, wheat and sesame allergens.

Distribution

Distributed from recalling firm's central kitchen to recalling firm's grocery store locations for direct-to-consumer sale.

Type: Voluntary: Firm initiated

Recall Initiated: 2022-05-16

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 76 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 (Dierbergs Central Kitchen) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.

How often does Dierbergs Central Kitchen have FDA actions?

This is the only FDA action we have on record for Dierbergs Central Kitchen in our database.

Where can I find the official FDA record?

The official record is available on FDA.gov. Search for "F-1131-2022" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.

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