Honeyville YELLOW COLOR
Reason Undeclared Red #40.
Montmorency Tart Cherry Concentrate 100% Juice 32-oz bottle recall
Recalled by King Orchards · Central Lake, MI, United States
Class II — Moderate risk. May cause temporary or reversible harm; serious harm unlikely.
Why it was recalled
Incorrect quantity of sugar listed in Nutrition Facts. Label states 1g sugar per serving when actually 15g per serving.
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
Montmorency Tart Cherry Concentrate 100% Juice 32-oz bottle (sold individual and 12 per case), 16-oz bottle (sold individual and 12 per case), and 1-oz packet (sold individual and per 25, 50, 100, 250, 300, and 1000)
Quantity: 1-oz Packets: 15,600; 16-oz Bottles: 1,332; 32-oz Bottles: 1420
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.
1-oz Packets, Lot: 18297, Best by: 05/2020. 16-oz Bottles, Lot: 1829701, Best by: Mar 2020. 32-oz Bottles, Lot: 1900401, 1900402, 1900403, Best by: May 2020.
Where it was sold
California Connecticut Florida Georgia Illinois Indiana Kentucky Louisiana Maryland Michigan Missouri North Carolina Nebraska New Mexico New York Ohio Pennsylvania South Carolina Wisconsin West Virginia
FDA's distribution note: CA, CT, FL, GA, IL, IN, KY, LA, MD, MI, MO, NC, NE, NM, NY, OH, PA, SC, 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
- King Orchards
- Initiated by
- Voluntary: Firm initiated
- Recall initiated
- Feb 12, 2019
- In FDA report of
- Mar 6, 2019
- Terminated
- Aug 6, 2019
- FDA recall number
- F-1054-2019 · event 82091
- Official record
- FDA enforcement report search
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