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.
La Centro Americana COMINO MOLIDO Ground Cumin recall
Recalled by La Centro Americana Corporation · Bay Shore, NY, United States
Class I — High risk. Reasonable probability of serious harm or death.
Why it was recalled
Cumin may contain undeclared peanut protein.
Undeclared allergen: Peanut
For someone with a food allergy the label is the only protection. An undeclared allergen can trigger a severe reaction even in a trace amount, which is why most of these recalls are Class I. All undeclared allergens recalls.
What was recalled
La Centro Americana COMINO MOLIDO Ground Cumin, Net Wt. 5 LBS held in clear plastic containers. Distributed by: La Centro Americana Corp. 2280 Union Blvd. Bay Shore, NY 11706 Tel. (631) 206-3097
Quantity: 6 units initially (5 units returned)
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.
none
Where it was sold
New York
FDA's distribution note: NY
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. The risk from an undeclared allergen is to people allergic to peanut; for anyone else the product is generally not a safety concern. 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
- La Centro Americana Corporation
- Initiated by
- Voluntary: Firm initiated
- Recall initiated
- Jan 23, 2015
- In FDA report of
- Mar 18, 2015
- Terminated
- May 9, 2017
- FDA recall number
- F-1414-2015 · event 70408
- Official record
- FDA enforcement report search
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