RecallHawk
Class I Recall

Grindsted SSD 6242 Stabilizer System, 22.68 kg/ 50 lb bag

Danisco USA Inc.

Summary

The FDA issued a Class I for Grindsted SSD 6242 Stabilizer System, 22.68 kg/ 50 lb bag by Danisco USA Inc.. Reason: Potential Salmonella Contamination.

Details

Source

Food Recall

External ID

F-1334-2024

Action Date

2024-06-12

Status

Terminated

Category

food

Product Description

Grindsted SSD 6242 Stabilizer System, 22.68 kg/ 50 lb bag

Lot/Code Info: Lot number: 1204600490

Quantity Affected: 884.52 kg

Reason for Recall

Potential Salmonella Contamination

Distribution

US: AZ, CA, CO, FL, IA, ID, IL, IN, KS, KY, MI, MN, MO, NE, NJ, NY, OH, OK, PA, TN, TX, UT, VA, WI; Canada, and Mexico

Type: Voluntary: Firm initiated

Recall Initiated: 2024-05-03

Company

Danisco USA Inc.

New Century, KS

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

Danisco USA Inc. has 36 FDA actions in our database, including 36 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 (Danisco USA Inc.) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.

How often does Danisco USA Inc. have FDA actions?

Danisco USA Inc. has 36 FDA actions in our database, including 36 recalls and 0 device clearances.

Where can I find the official FDA record?

The official record is available on FDA.gov. Search for "F-1334-2024" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.

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