Food Recall Check
Class I · High risk Terminated Initiated Feb 25, 2013 (14 years ago)

GREEN DAY brand White Melon Seeds recall

Recalled by Domega NY International Co Ltd · Brooklyn, NY, United States

Class I — High risk. Reasonable probability of serious harm or death.

Why it was recalled

The product contained undeclared sulfites (1539 ppm) based on sampling & analysis by New York State Department of Agriculture & Markets.

A label that does not match the product can hide an ingredient someone must avoid, or show a wrong use-by date. All labeling errors recalls.

What was recalled

GREEN DAY brand White Melon Seeds, Net Wt. 9.8 oz (280g) , UPC 6 868978 724120, Produce of P.R.C. --- Firms on Label: Manufacturer: Jiangmen Xinhui Parksun Food Co., Ltd. Add: Donggua Hill, Beltou Village, Qibao, Xinhui District, Jiangmen City, Guangdong -- Packed For: Domega NY International Co., ltd. 1915 West 13th Street Brooklyn, N.Y. 11223 --- Nutrition Facts: Serving Size (illegible) Servings Per Container 4 --- The product is packaged in a clear, plastic bag on a plastic tray insert.

Quantity: 37 cases (30 x 280 gram packages per case)

Food: Nuts & seeds Fresh fruit

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.

MFD 09/30/2013 EXP 09/29/2014

Where it was sold

New York

FDA's distribution note: New York City

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. 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
Domega NY International Co Ltd
Initiated by
Voluntary: Firm initiated
Recall initiated
Feb 25, 2013
In FDA report of
Apr 17, 2013
Terminated
Apr 5, 2013
FDA recall number
F-1302-2013 · event 64467
Official record
FDA enforcement report search

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