Frog Hollow Holiday Fruitcake Incorrect ingredients recall
Recalled by Frog Hollow Farm · Brentwood, CA, United States
Class II — Moderate risk. May cause temporary or reversible harm; serious harm unlikely.
Why it was recalled
Customer alerted firm that walnuts were listed on the web page but not in the ingredient label
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
Frog Hollow Holiday Fruitcake Incorrect ingredients: Organic butter, organic flour, organic sugar, organic eggs, molasses, candied orange peel, rum, dried plums, organic dried peaches. Correct label: organic butter, organic flour, organic sugar, organic eggs, organic walnuts, molasses, candied orange peel, rum, organic dried plums, organic dried peaches, organic milk, salt, baking soda, cinnamon.
Quantity: 60 cakes
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.
Purchased between June 13, 2019 and November 15, 2019
Where it was sold
California Connecticut District of Columbia Florida Illinois Kansas Kentucky Louisiana Massachusetts Missouri North Dakota New Jersey New Mexico New York Ohio Oklahoma Oregon South Carolina Tennessee Texas Virginia Washington
FDA's distribution note: CA, CT, DC, FL, IL, KS, KY, LA, MA, MO, ND, NJ, NM, NY, OH, OK, OR, SC, TN, TX, VA, WA
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
- Frog Hollow Farm
- Initiated by
- Voluntary: Firm initiated
- Recall initiated
- Nov 21, 2019
- In FDA report of
- Dec 11, 2019
- Terminated
- Feb 3, 2020
- FDA recall number
- F-0210-2020 · event 84351
- Official record
- FDA enforcement report search