Spicy Black Bean Burger powder mix recall
Recalled by Coalescence LLC · Columbus, OH, United States
Class II — Moderate risk. May cause temporary or reversible harm; serious harm unlikely.
Why it was recalled
Undeclared peanuts in spicy black bean burger powder mix.
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
Spicy Black Bean Burger powder mix, packaged in 30 LB poly-lined Kraft bags.
Quantity: 218,310 lbs
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.
The following lots are affected by this recall: C17SEP2014B95, C18SEP2014B102, C23SEP2014B123, C10OCT2014B195, C13OCT2014B203, C14OCT2014B207, C18OCT2014B223, C20OCT2014B229, C24OCT2014B250, C28OCT2014B265, C01NOV2014B287, C04NOV2014B296, C05NOV2014B299, C03DEC2014B401, C03DEC2014B402, C05DEC2014B414, C09DEC2014B432, C11DEC2014B440, C12DEC2014B450, C19DEC2014B473, C20DEC2014B481, and C23DEC2014B481.
Where it was sold
Michigan Ohio Utah
FDA's distribution note: The affected product was distributed to three consignees in Ohio, Utah, and Michigan.
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. 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
- Coalescence LLC
- Initiated by
- Voluntary: Firm initiated
- Recall initiated
- Dec 24, 2014
- In FDA report of
- Jul 15, 2015
- Terminated
- Sep 17, 2015
- FDA recall number
- F-2819-2015 · event 70135
- Official record
- FDA enforcement report search