Meijer Express Dark Chocolate Covered Almonds, 7.5oz plastic cup with lid, UPC 7-60236-19787-4
Summary
The FDA issued a Class I for Meijer Express Dark Chocolate Covered Almonds, 7.5oz plastic cup with lid, UPC 7 by Meijer Inc. Reason: undeclared milk.
Details
Source
Food Recall
External ID
F-0975-2023
Action Date
2023-06-14
Status
Terminated
Category
food
Product Description
Meijer Express Dark Chocolate Covered Almonds, 7.5oz plastic cup with lid, UPC 7-60236-19787-4
Lot/Code Info: All sell by dates
Quantity Affected: 9,030 - EACHES
Reason for Recall
undeclared milk
Distribution
The recall includes stand-up pouches carried at Meijer stores and to-go cups carried at Meijer Express locations in Michigan, Indiana, Illinois, Ohio, Kentucky, and Wisconsin.
Type: Voluntary: Firm initiated
Recall Initiated: 2023-05-19
Company
Grand Rapids, MI
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 32 food recalls issued in the same week, part of 204 food-related FDA actions this month.
Meijer Inc has 18 FDA actions in our database, including 18 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 (Meijer Inc) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.
How often does Meijer Inc have FDA actions?
Meijer Inc has 18 FDA actions in our database, including 18 recalls and 0 device clearances.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "F-0975-2023" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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