Mary's Harvest brand, Celery Peanut Butter Cup G&G, net wt. per cup 7.5 oz., UPC 8 87241 79672 1
Summary
The FDA issued a Class I for Mary's Harvest brand, Celery Peanut Butter Cup G&G, net wt. per cup 7.5 oz., UPC by Mary's Harvest Fresh Foods, Inc.. Reason: Potential contamination with Salmonella..
Details
Source
Food Recall
External ID
F-1133-2022
Action Date
2022-06-08
Status
Terminated
Category
food
Product Description
Mary's Harvest brand, Celery Peanut Butter Cup G&G, net wt. per cup 7.5 oz., UPC 8 87241 79672 1
Lot/Code Info: Use By Dates Range: 05/15/2022 to 05/31/2022
Quantity Affected: Celery Peanut Butter cup: 58 cases (6/7.5 oz. cups per case) or 348 cups.
Reason for Recall
Potential contamination with Salmonella.
Distribution
Distributed in OR and WA.
Type: Voluntary: Firm initiated
Recall Initiated: 2022-05-23
Company
Portland, OR
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 76 food recalls issued in the same week, part of 204 food-related FDA actions this month.
Mary's Harvest Fresh Foods, Inc. has 2 FDA actions in our database, including 2 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 (Mary's Harvest Fresh Foods, Inc.) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.
How often does Mary's Harvest Fresh Foods, Inc. have FDA actions?
Mary's Harvest Fresh Foods, Inc. has 2 FDA actions in our database, including 2 recalls and 0 device clearances.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "F-1133-2022" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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