Albanese Dark Chocolate Espresso Bean packaged into 9oz plastic tubs 12 tubs per case
Summary
The FDA issued a Class I for Albanese Dark Chocolate Espresso Bean packaged into 9oz plastic tubs 12 tubs p by Albanese Confectionery Group, Inc.. Reason: Undeclared Allergen - Peanut.
Details
Source
Food Recall
External ID
F-0864-2022
Action Date
2022-03-23
Status
Terminated
Category
food
Product Description
Albanese Dark Chocolate Espresso Bean packaged into 9oz plastic tubs 12 tubs per case
Lot/Code Info: Lot No. LB1111514X1 Item No. 63143 UPC Code 634418621436
Quantity Affected: 756 tubs
Reason for Recall
Undeclared Allergen - Peanut
Distribution
A single distribution center in IN
Type: Voluntary: Firm initiated
Recall Initiated: 2022-03-09
Company
Merrillville, IN
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 122 food recalls issued in the same week, part of 204 food-related FDA actions this month.
Albanese Confectionery Group, Inc. has 3 FDA actions in our database, including 3 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 (Albanese Confectionery Group, Inc.) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.
How often does Albanese Confectionery Group, Inc. have FDA actions?
Albanese Confectionery Group, Inc. has 3 FDA actions in our database, including 3 recalls and 0 device clearances.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "F-0864-2022" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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