Food Recall Check
Class I · High risk Terminated Initiated Feb 3, 2014 (13 years ago)

Humei Foods DRIED LILY recall

Recalled by Humei Trading Inc. · Jamaica, NY, United States

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

Why it was recalled

The product contained undeclared sulfites (409.1 ppm) based on sampling and 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

Humei Foods DRIED LILY, Net Wt. 340 g 12 oz +- 5 g -- PRODUCT OF CHINA --- Firms on label: Shanghai Dingmei International Trade Co., LTD, Add: Room 516B, No. 1218, Walma Road, Shanghai, China 200011 Tel: 86 21 33761911 Fax: 86 21 33761933 -- Shanghai Huipu Food Co., LTD, Add: No. 4545, Daye Highway, Fengxian, Shanghai, China 201404 Tel: 86 21 57488229 Fax: 86 21 57489557 -- Distributed By: Humei Trading INC (New York), Add: 1811 Neck Road, Brooklyn, NY 11229 Tel: 1 646 708 6758 --- Nutrition Facts: Serving Size 50 g, Serving About 3

Quantity: 30 x 12 oz. packages

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.

No coding

Where it was sold

New York

FDA's distribution note: Flushing, 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. 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
Humei Trading Inc.
Initiated by
Voluntary: Firm initiated
Recall initiated
Feb 3, 2014
In FDA report of
Jul 16, 2014
Terminated
Jul 8, 2014
FDA recall number
F-2085-2014 · event 67425
Official record
FDA enforcement report search