Recalled Meltaways product is packaged in clear cellophane bags recall
Recalled by Cranberry Sweets & More Inc · Coos Bay, OR, United States
Class I — High risk. Reasonable probability of serious harm or death.
Why it was recalled
Peanut Butter Meltaway was mis-labeled as Mint Meltaways and peanut is undeclared.
Undeclared allergen: Peanut
For someone with a food allergy the label is the only protection. An undeclared allergen can trigger a severe reaction even in a trace amount, which is why most of these recalls are Class I. All undeclared allergens recalls.
What was recalled
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.
Quantity: 300 lbs.
Lot codes, dates and UPCs
A recall covers only these codes. Compare them with the lot number, best-by date or UPC printed on your package.
Code: 032123
Where it was sold
Nationwide.
Oregon Washington
FDA's distribution note: Distributed to stores in Oregon and Washington and sold nationwide through direct orders.
Do not eat it. Class I means FDA judged there is a reasonable probability of serious illness or death. If the brand, size and lot or date code on your package match, throw the product away or return it to the store for a refund, and clean any surface or container it touched. If anyone has eaten it and feels unwell, contact a doctor and mention the recall. The risk from an undeclared allergen is to people allergic to peanut; for anyone else the product is generally not a safety concern. FDA lists this recall as terminated: the company has finished removing the product, so it should no longer be on shelves - but it can still be in a freezer or pantry.
- Recalling firm
- Cranberry Sweets & More Inc
- Initiated by
- Voluntary: Firm initiated
- Recall initiated
- Dec 5, 2022
- In FDA report of
- Jan 11, 2023
- Terminated
- Feb 9, 2023
- FDA recall number
- F-0214-2023 · event 91277
- Official record
- FDA enforcement report search