Recalled Meltaways product is packaged in clear cellophane bags, net wt. 4oz and 8 oz. and has no UPC. The front label
Summary
The FDA issued a Class I for Recalled Meltaways product is packaged in clear cellophane bags, net wt. 4oz and by Cranberry Sweets & More Inc. Reason: Peanut Butter Meltaway was mis-labeled as Mint Meltaways and peanut is undeclared..
Details
Source
Food Recall
External ID
F-0214-2023
Action Date
2023-01-11
Status
Terminated
Category
food
Product Description
Recalled Meltaways product is packaged in clear cellophane bags, net wt. 4oz and 8 oz. and has no UPC. The front label is read Mint Meltaways, Cranberry Sweets and more, Coos Bay, OR 97402. The back label is read Heirloom Mint Meltaways, Ingredients: Milk Chocolate (***soy lecithin***), Oregon peppermint oil. Contains the following allergens: Milk, Soy.
Lot/Code Info: Code: 032123
Quantity Affected: 300 lbs.
Reason for Recall
Peanut Butter Meltaway was mis-labeled as Mint Meltaways and peanut is undeclared.
Distribution
Distributed to stores in Oregon and Washington and sold nationwide through direct orders.
Type: Voluntary: Firm initiated
Recall Initiated: 2022-12-05
Company
Coos Bay, 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 17 food recalls issued in the same week, part of 204 food-related FDA actions this month.
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 (Cranberry Sweets & More Inc) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.
How often does Cranberry Sweets & More Inc have FDA actions?
This is the only FDA action we have on record for Cranberry Sweets & More Inc in our database.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "F-0214-2023" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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