Chocolate Peanut Butter Cup. Product were available for purchase at the following banner: Haggen. Packaged in clear pl
Summary
The FDA issued a Class I for Chocolate Peanut Butter Cup. Product were available for purchase at the followi by Albertsons Companies LLC. Reason: Potential Salmonella contamination..
Details
Source
Food Recall
External ID
F-1328-2022
Action Date
2022-06-29
Status
Terminated
Category
food
Product Description
Chocolate Peanut Butter Cup. Product were available for purchase at the following banner: Haggen. Packaged in clear plastic cup overwrapped in plastic. Net wt. 5 oz.
Lot/Code Info: All Sell thru Dates up to and including May 20, 22.
Quantity Affected: Firm did not provide
Reason for Recall
Potential Salmonella contamination.
Distribution
The store prepared products were available and sold in the following states: Alaska, Arkansas, California, Colorado, Connecticut, Delaware, Hawaii, Idaho, Illinois, Indiana, Iowa, Louisiana, Maine, Maryland, Massachusetts, Nebraska, Nevada, New Hampshire, New Jersey, New Mexico, New York, North Dakota, Oregon, Pennsylvania, Rhode Island, South Dakota, Texas, Utah, Vermont, Virginia, Washington, and Wyoming.
Type: Voluntary: Firm initiated
Recall Initiated: 2022-05-21
Company
Boise, ID
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.
Albertsons Companies LLC has 174 FDA actions in our database, including 174 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 (Albertsons Companies LLC) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.
How often does Albertsons Companies LLC have FDA actions?
Albertsons Companies LLC has 174 FDA actions in our database, including 174 recalls and 0 device clearances.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "F-1328-2022" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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