Hexing Haw Balls candy
Reason Unapproved dye Ponceau 4R
Moonwalk 70% dark chocolate bar recall
Recalled by Cocanu LLC · Portland, OR, United States
Class II — Moderate risk. May cause temporary or reversible harm; serious harm unlikely.
Why it was recalled
Lactose is declared but milk is not declared on label.
Undeclared allergen: Milk
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
Moonwalk 70% dark chocolate bar. It is packaged in white shiny paper with blue print. Net Weight: 1.2 oz / 35gr. No UPC. The label is read in parts: "***Moonwalk ***a 70% dark chocolate bar ***chocolate, cacao nibs and pop rocks ***Contents: cacao beans, cacao butter, cane sugar, pop rocks (sugar, lactose, corn syrup, flavoring)***cloudforest Portland, OR***cloudforest.shop***".
Quantity: 852 bars
Food: Chocolate & candy
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.
Lot 683 (Best by 8/26/2021) Lot 690 (Best by 12/15/2021) Lot 695 (Best by 12/30/2021) Lot 703 (Best by 2/11/2022) Lot 709 (Best by 3/10/2022) Lot 722 (Best by 5/28/2022)
Where it was sold
California Oregon
FDA's distribution note: Distributed in CA and OR.
Check the codes, then return or discard. Class II means eating it may cause temporary or reversible health problems. If your package matches the recalled codes, do not eat it - return it to the store or throw it away. The risk from an undeclared allergen is to people allergic to milk; 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
- Cocanu LLC
- Initiated by
- Voluntary: Firm initiated
- Recall initiated
- Aug 3, 2021
- In FDA report of
- Aug 25, 2021
- Terminated
- May 13, 2022
- FDA recall number
- F-0867-2021 · event 88414
- Official record
- FDA enforcement report search
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