Hexing Haw Balls candy
Reason Unapproved dye Ponceau 4R
Winfield's CWB Chocolate Bar recall
Recalled by Chocolate Bar Holdings LLC · Houston, TX, United States
Class II — Moderate risk. May cause temporary or reversible harm; serious harm unlikely.
Why it was recalled
Undeclared milk allergen.
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
Winfield's CWB Chocolate Bar, packed in clear cello bag with fabric bow on top. Manufactured by CBSL Commissary (DBA Winfield's Chocolate Bar) 9127 Stella Link Rd Houston Texas. Multiple product shapes/sizes: 1) Cat, Net wt. 8oz (226.8g), UPC: 00810079833030, Unit size 5 x 3 1/2 x 2. 2) Teddy Bear, Net wt. 8oz (226.8g), UPC: 00810079833405, Unit size 5 1/2 x 2 1/2 x 2. 3) Easter Bunny, Net wt. 16oz (453.59g), UPC: 00810079837892, Unit size 4 x 1 x 8 1/2.
Quantity: 24 total units (various shapes/sizes)
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.
No lot numbers are on these products, so the firm's recall scope is for the entire production line for the following product numbers: 00810079833030 00810079833405 00810079837892
Where it was sold
Texas
FDA's distribution note: Houston, TX
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 completed: 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
- Chocolate Bar Holdings LLC
- Initiated by
- Voluntary: Firm initiated
- Recall initiated
- Apr 27, 2026
- In FDA report of
- Jul 22, 2026
- FDA recall number
- H-1156-2026 · event 98931
- Official record
- FDA enforcement report search
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