Maple flavored lipid-based inclusions recall
Recalled by SensoryEffects Powder Systems · Defiance, OH, United States
Class II — Moderate risk. May cause temporary or reversible harm; serious harm unlikely.
Why it was recalled
The firm was notified by a customer that a random sample from lot 2013-36707 tested positive for Salmonella.
Pathogen: Salmonella
Salmonella is the most common cause of food recalls for bacteria, often in eggs, produce, nuts and spices.
The most serious food recalls: a contaminated product can cause outbreaks, hospitalisations and deaths, especially for pregnant people, young children, older adults and anyone with a weakened immune system. All bacteria & viruses recalls.
What was recalled
Maple flavored lipid-based inclusions. Maple NT-RF and Maple NT-MF, NET WT: 50 lbs, Ingredients: Sugar, vegetable oil (palm, palm kernel), wheat flour, cocoa powder, glucose, extractives of foenugreek, maple sugar, caramel color, soy lecithin. SensoryEffects¿¿ , 136 Fox Run Dr., Defiance, OH 43512
Quantity: Lot 2013-36707 120/50 lb boxes. Lot 2013-36708 247/50 lb boxes
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.
Item code 20526 Maple NT-RF lot 2013-36707 and Item code 20525 Maple NT-MF lot 2013-36708
Where it was sold
Kentucky Minnesota South Dakota Washington
FDA's distribution note: Product was shipped to the following states: KY, MN, SD, WA. Product was also shipped to Canada.
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
- SensoryEffects Powder Systems
- Initiated by
- Voluntary: Firm initiated
- Recall initiated
- Jul 20, 2013
- In FDA report of
- Aug 28, 2013
- Terminated
- Nov 5, 2013
- FDA recall number
- F-1848-2013 · event 65845
- Official record
- FDA enforcement report search