Food Recall Check
Class II · Moderate risk Terminated Initiated May 13, 2016 (10 years ago)

Haitai Matdongsan Peanuts Crunch Snack recall

Recalled by H & E Trading Inc · Wyckoff, NJ, United States

Class II — Moderate risk. May cause temporary or reversible harm; serious harm unlikely.

Why it was recalled

Haiati Matdongsan Peanut Crunch Snack, 80g and 325g, plastic flex bag is being recalled because it contains Soy Lecithin and this was not listed on the finished product labeling.

Undeclared allergens: Peanut Soy

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

Haitai Matdongsan Peanuts Crunch Snack, Net Wt. 11.49 oz. (325gr), Imported and Distributed by: Haitai, Inc, 7227 Telegraph Road, Montebello, CA 90640 - H & E Trading Inc, 514 Eugene Way, Wyckoff, NJ 07481, UPC 8 801019606786

Quantity: 3,115 cases

Food: Nuts & seeds Chips & snacks

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.

Expiration dates: 9/29/2016, 1/13/2017, 2/7/2017, 3/1/2017 and 3/8/2017

Where it was sold

Georgia Massachusetts Maryland New Jersey New York Pennsylvania Virginia

FDA's distribution note: GA, MA, MD, NJ, NY, PA and VA

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, soy; 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
H & E Trading Inc
Initiated by
Voluntary: Firm initiated
Recall initiated
May 13, 2016
In FDA report of
Aug 24, 2016
Terminated
Feb 14, 2018
FDA recall number
F-1937-2016 · event 74611
Official record
FDA enforcement report search

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