RecallHawk
Class I Recall

1. SALTED NUT ROLL PRE-MADE FUDGE (6SS) 6LB NET WT - not consumer package, bulk carton

Calico Cottage Inc

Summary

The FDA issued a Class I for 1. SALTED NUT ROLL PRE-MADE FUDGE (6SS) 6LB NET WT - not consumer package, bulk by Calico Cottage Inc. Reason: Fudge contains peanut butter that is potentially contaminated with Salmonella..

Details

Source

Food Recall

External ID

F-1340-2022

Action Date

2022-06-29

Status

Terminated

Category

food

Product Description

1. SALTED NUT ROLL PRE-MADE FUDGE (6SS) 6LB NET WT - not consumer package, bulk carton

Lot/Code Info: GTIN: 00673305060095 LOT: 22049037, 22054034, 22063017, 22089043, 22101071, 22108193, 22133422

Quantity Affected: 677 units (total)

Reason for Recall

Fudge contains peanut butter that is potentially contaminated with Salmonella.

Distribution

Nationwide

Type: Voluntary: Firm initiated

Recall Initiated: 2022-05-24

Company

Calico Cottage Inc

Amityville, NY

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

Calico Cottage Inc has 4 FDA actions in our database, including 4 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 (Calico Cottage Inc) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.

How often does Calico Cottage Inc have FDA actions?

Calico Cottage Inc has 4 FDA actions in our database, including 4 recalls and 0 device clearances.

Where can I find the official FDA record?

The official record is available on FDA.gov. Search for "F-1340-2022" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.

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