1. PEANUT BUTTER FUDGE (3 - 6LB SLABS/CS) 18LB NET WT - not consumer packaging, bulk carton 2. PEANUT BUTTER FUDGE (6S)
Summary
The FDA issued a Class I for 1. PEANUT BUTTER FUDGE (3 - 6LB SLABS/CS) 18LB NET WT - not consumer packaging, by Calico Cottage Inc. Reason: Fudge contains peanut butter that is potentially contaminated with Salmonella..
Details
Source
Food Recall
External ID
F-1338-2022
Action Date
2022-06-29
Status
Terminated
Category
food
Product Description
1. PEANUT BUTTER FUDGE (3 - 6LB SLABS/CS) 18LB NET WT - not consumer packaging, bulk carton 2. PEANUT BUTTER FUDGE (6S) 6LB NET WT- not consumer packaging, bulk carton 3. PEANUT BUTTER FUDGE (6SS) 6LB NET WT- not consumer packaging, bulk carton
Lot/Code Info: 1. GTIN: 00673305110929 22069040, 22108197, 22118291 2. GTIN 00673305110554 22130390 3. GTIN: 00673305058047 22053035, 22061020, 22062031, 22089049, 22101072, 22105162, 22112236
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
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-1338-2022" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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