Horizon Organic ORG ASEP CHOC MILK 1%
Reason Product has the potential to be spoiled.
Butter Toffee net wt recall
Recalled by 4 J's Treats, LLC dba Bruttles Gourmet Candies · Spokane Valley, WA, United States
Class II — Moderate risk. May cause temporary or reversible harm; serious harm unlikely.
Why it was recalled
The Butter Toffee, 16oz box, declares butter but does not declare milk. Label does not declare soy which is present in the non-stick spray being used on the Butter Toffee production trays. The Butter Toffee, 4oz part of the SAMPLERS package, declares butter but does not declare milk, and it does not declare soy which is present in the non-stick spray being used on the Butter Toffee production trays.
A label that does not match the product can hide an ingredient someone must avoid, or show a wrong use-by date. All labeling errors recalls.
What was recalled
Butter Toffee, net wt. 16 oz, 6 units per case. Label declares: Butter Toffee, Butter, Sugar, Corn Syrup, Almonds, Vanilla, Salt. www.bruttles.com. Butter Toffee, net wt. 4oz., part of Medium Samplers package. Product is packaged in cello bag and labeled Butter Toffee. Label declares: Butter Toffee, Butter, Sugar, Corn Syrup, Almonds, Vanilla, Salt. www.bruttles.com.
Quantity: 25 boxes of Butter Toffee. 120 boxes of Samplers.
Food: Milk & dairy
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.
None
Where it was sold
Washington
FDA's distribution note: distributed in Washington
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
- 4 J's Treats, LLC dba Bruttles Gourmet Candies
- Initiated by
- Voluntary: Firm initiated
- Recall initiated
- Feb 28, 2023
- In FDA report of
- Mar 29, 2023
- Terminated
- Mar 23, 2023
- FDA recall number
- F-0647-2023 · event 91828
- Official record
- FDA enforcement report search
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