Honeyville YELLOW COLOR
Reason Undeclared Red #40.
Wawa COLD BREW COFFEE***ONE PINT recall
Recalled by Royal Ice Cream Company · Cleveland, OH, United States
Class I — High risk. Reasonable probability of serious harm or death.
Why it was recalled
Product is being recalled due to undeclared peanuts.
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
Wawa COLD BREW COFFEE***ONE PINT (473ML)***MADE WITH WAWA COLD BREW***Nutrition Facts***INGREDIENTS: CREAM, SKIM MILK, LIQUID SUGAR (SUGAR, WATER), CORN SYRUP, WHEY, COFFEE, GUAR GUM, LOCUST BEAN GUM, TARA GUM, CARAMEL COLOR CONTAINS: MILK*DISTRIBUTED BY WAWA, INC, WAWA, PA 19063
Quantity: 1000 pints
Food: Juice & beverages
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.
22094 11:27-16:02
Where it was sold
District of Columbia Delaware Florida Maryland New Jersey Pennsylvania Virginia Washington
FDA's distribution note: Delaware, Florida, Maryland, New Jersey, Pennsylvania, Virginia and Washington DC.
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
- Royal Ice Cream Company
- Initiated by
- Voluntary: Firm initiated
- Recall initiated
- Jun 7, 2022
- In FDA report of
- Jul 20, 2022
- Terminated
- Jul 19, 2022
- FDA recall number
- F-1413-2022 · event 90413
- Official record
- FDA enforcement report search
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