Hexing Haw Balls candy
Reason Unapproved dye Ponceau 4R
Heilemann Confiserie Wehnachtsfiguren Aus… recall
Recalled by Alpenland International, Inc. · Cleveland, GA, United States
Class II — Moderate risk. May cause temporary or reversible harm; serious harm unlikely.
Why it was recalled
The manufacturer informed the firm that they received a complaint of plastic in the product.
Hard or sharp fragments can cut the mouth or throat, break teeth or cause choking. They usually come from equipment wear or packaging on the production line. All foreign material recalls.
What was recalled
HEILEMANN CONFISERIE WEHNACHTSFIGUREN AUS EDELVOLLMILCH-SCHOKOLADE Solid Chocolate Holiday Treats 3.5 oz box UPC 4006574007199
Quantity: 220/3.5 oz boxes
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.
Best if Used By 17.05.23 and 17.08.23
Where it was sold
Alabama Arizona California Colorado Florida Georgia Idaho Illinois Indiana Kansas Maryland Michigan Minnesota Missouri Mississippi North Carolina New Hampshire New Jersey New York Ohio Oklahoma Pennsylvania South Carolina Tennessee Texas Utah Virginia Washington Wisconsin West Virginia
FDA's distribution note: Product was shipped to the following states: AL, AZ, CA, CO, FL, GA, ID, IL, IN, KS, MD, MI, MN, MO, MS, NC, NH, NJ, NY, OH, OK, PA, SC, TN, TX, UT, VA, WA, WI & WV.
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. 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
- Alpenland International, Inc.
- Initiated by
- Voluntary: Firm initiated
- Recall initiated
- Jan 25, 2023
- In FDA report of
- Mar 8, 2023
- Terminated
- Jun 23, 2023
- FDA recall number
- F-0383-2023 · event 91565
- Official record
- FDA enforcement report search
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