FDA recall record

Rong Shing Trading NY Glam Day Nougat Candy packaged in 6-ounce recall — FDA F-0097-2020

Product may contain undeclared allergens, specifically milk and eggs.

Class Iclassification
F-0097-2020official record ID
Nov 6, 2019report date

Recall record at a glance

Official recordF-0097-2020
CategoryFood Recalls
ClassificationClass I
FDA record statusTerminated
Recalling firmRong Shing Trading NY Inc.
Report dateNov 6, 2019
Recall initiation dateOct 1, 2019
Quantity57 cases; 30 packages/cases (1,710 packages total)
LocationBrooklyn, NY, United States

Official product description

Glam Day Nougat Candy packaged in 6-ounce (170g) plastic packages containing individually wrapped units identified only as NOUGAT. 30 plastic packages per master case. The 6-ounce plastic bags listed the following codes: BEST BEFORE 10/15/2020; UPC 6 950296 804834. Ingredients: Peanuts, Sugar, liquid Glucose, Malt Sugar, Starch (Cereals Containing Gluten), Salt. Allergies: Contains Peanuts. Manufacturer: Jiangmen Xinhui Green Day Food Co., Ltd., Add: No. 1 Donggua Hill, Beitou Village, Qibao, Xinhui District, Jiangmen City, Guangdong. Glam Day International Corp., 47-57 Bridgewater Brooklyn, NY 11222.

Why the product was recalled

Product may contain undeclared allergens, specifically milk and eggs.

Distribution information

Retailers in 17 states: CO, FL, GA, IL, KY, LA, MA, MD, MO, NC, NY, OH, OR, PA, TN, TX, and WI

How to read the classification

FDA Class I indicates a situation in which there is a reasonable probability that use of or exposure to the product will cause serious adverse health consequences or death. The classification shown here comes directly from the FDA enforcement record.

Additional record details

Recall type: Voluntary: Firm initiated. Initial notification: Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit.

What to do next

If you believe you have the recalled product, use the recall number and firm information above to confirm the official notice and follow the instructions issued by the FDA, recalling firm, retailer or product manufacturer. For drugs and medical devices, decisions about treatment or medical care should be discussed with a qualified health professional.

About this record

Recall Lookup USA preserves the most complete source information successfully retrieved. We do not create missing facts or infer affected lots or VINs. The official record may still change, so use the identifier above when verifying current instructions.

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