Dr. Praeger's Sensible Foods Bombay Curry Veggie Burgers
Reason Ungar's Food Products Inc. was notified by a supplier that cumin, an ingredient in the Bombay Curry Veggie Burger, tested positive for peanut protein.
Dr. Praeger's California Veggie Burgers Gluten Free recall
Recalled by Ungar's Food Products, Inc. · Elmwood Park, NJ, United States
Class I — High risk. Reasonable probability of serious harm or death.
Why it was recalled
Dr. Praeger's Gluten Free California Burgers contain undeclared soy.
Undeclared allergens: Soy Wheat
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
Dr. Praeger's California Veggie Burgers Gluten Free 11 oz. Manufactured by Dr. Praeger's Sensible Foods Elmwood Park, NJ 07047 www.drpraegers.com Made in the USA UPC 080868000602
Quantity: 11,400 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.
Case Lot F15BC-04A Retail Box Lot # F15BC
Where it was sold
Nationwide.
FDA's distribution note: Nationwide
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 soy, wheat; 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
- Ungar's Food Products, Inc.
- Initiated by
- Voluntary: Firm initiated
- Recall initiated
- Jun 1, 2015
- In FDA report of
- Jul 22, 2015
- Terminated
- Apr 21, 2016
- FDA recall number
- F-2852-2015 · event 71381
- Official record
- FDA enforcement report search