Pumpkin Spice No Bake Cookie
Reason Peanuts & Eggs. The firm list peanuts in the ingredient statement but omitted them from the contain statement. They also have eggs listed in the contain statement but there are no eggs in the product.
Ground cinnamon recall
Recalled by Kalustyan Corp. · Union, NJ, United States
Class I — High risk. Reasonable probability of serious harm or death.
Why it was recalled
Possible Salmonella contamination in cinnamon
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
Ground cinnamon. Packaged in bulk 50 lb. corrugated boxes with inside liner.
Quantity: 243 boxes (12,150 pounds)
Food: Spices & seasonings
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.
Original manufactured lot # 165089 which was divided into 4 smaller lots: lot # 175742(7/6/20), lot # 173326 (5/11/20), lot # 174291 (6/1/20) & lot # 174382 (6/8/20).
Where it was sold
Illinois Texas
FDA's distribution note: Distributed in bulk to TX and IL in the US. Distributed to foreign facilities in Canada and Costa Rica
Do not eat it. Class I means FDA judged there is a reasonable probability of serious illness or death. If the brand, size and lot or date code on your package match, throw the product away or return it to the store for a refund, and clean any surface or container it touched. If anyone has eaten it and feels unwell, contact a doctor and mention the recall. 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
- Kalustyan Corp.
- Initiated by
- Voluntary: Firm initiated
- Recall initiated
- Sep 23, 2020
- In FDA report of
- Oct 14, 2020
- Terminated
- Dec 2, 2021
- FDA recall number
- F-0005-2021 · event 86472
- Official record
- FDA enforcement report search
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