America's Best (jeera) Cumin Powder
Reason The product was found to contain undeclared peanut protein on four occasions (11700 PPM, 2500 PPM, 86.9 PPM & 69.85 PPM) based on sampling and analysis by New York State Department of Agriculture & Markets
America's Best Corriander Powder recall
Recalled by Patel Grocery Corp · Brooklyn, NY, United States
Class I — High risk. Reasonable probability of serious harm or death.
Why it was recalled
The product was found to contain undeclared peanut allergens based on sampling and analysis by New York State Department of Agriculture & Markets.
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
AMERICA'S BEST CORRIANDER POWDER, NET WT.: 1) 7 OZ, 2) 14 OZ. (400 GMS) and 3) 28 OZ, sealed in plastic bags, Packed by Patel Grocery 5303 4th Ave. Brooklyn, NY 11220
Quantity: unable to determine as per NYSDAM
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
- Patel Grocery Corp
- Initiated by
- Voluntary: Firm initiated
- Recall initiated
- May 4, 2015
- In FDA report of
- Aug 19, 2015
- Terminated
- Aug 26, 2015
- FDA recall number
- F-2960-2015 · event 71817
- Official record
- FDA enforcement report search