Glam Day Nougat Candy Recall: Undeclared Milk and Egg Allergens
Rong Shing Trading NY Inc recalls Glam Day Nougat Candy (6oz plastic packages) due to potential undeclared milk and egg allergens. Consumers should check for best before date 10/15/2020 and UPC 6950296804834.
Lower-risk recall
Product may contain undeclared allergens, specifically milk and eggs.
Contact the company
What happened, in plain English
Rong Shing Trading NY Inc is recalling Glam Day Nougat Candy because it may contain undeclared milk and egg allergens. This poses a risk for people with allergies to these ingredients, especially those who are sensitive or have severe reactions. Read more at govinfonow.com/recall/16535-glam-day-nougat-candy-recall-undeclared-milk-and-egg-allergens.
Source Summary by GovInfoNow · govinfonow.com/recall/16535-glam-day-nougat-candy-recall-undeclared-milk-and-egg-allergens · Updated October 5, 2026 · FDA enforcement record: FDA #F-0097-2020
Cite this page
“Glam Day Nougat Candy Recall: Undeclared Milk and Egg Allergens.” GovInfoNow, updated October 5, 2026. https://govinfonow.com/recall/16535-glam-day-nougat-candy-recall-undeclared-milk-and-egg-allergens. Based on FDA recall #F-0097-2020 (https://api.fda.gov/food/enforcement.json?search=recall_number:%22F-0097-2020%22&limit=1).
Why it’s dangerous
The candy may contain undeclared milk and egg allergens, which can cause allergic reactions in sensitive individuals. The product is packaged in plastic bags with specific identifiers that help consumers identify the recalled items.
Who’s affected
People with milk or egg allergies are at risk. This recall affects consumers who purchased the 6-ounce plastic packages with the best before date of 10/15/2020.
How to tell if you have this one
Check for 6-ounce plastic packages with the best before date 10/15/2020 and UPC code 6950296804834. The product is labeled as NOUGAT with ingredients including peanuts and gluten.
- Brand
Glam Day- Product
Glam Day Nougat Candy packaged in 6-ounce (170g) plastic packages containing individually wrapped units identified only- Category
Food
What to do — step by step
Check Product Details
Look for the best before date 10/15/2020 and UPC 6950296804834 on the packaging.
Where it went and when
Where it was distributed
Distributed in 17 states.
FDA distribution: “Retailers in 17 states: CO, FL, GA, IL, KY, LA, MA, MD, MO, NC, NY, OH, OR, PA, TN, TX, and WI” States read from FDA’s own wording; “not listed” means the notice does not name it.
States: Colorado, Florida, Georgia, Illinois, Kentucky, Louisiana, Maryland, Massachusetts, Missouri, New York, North Carolina, Ohio, Oregon, Pennsylvania, Tennessee, Texas, Wisconsin.
Recall timeline
FDA terminated this recall 18 months after the firm started it.
- Firm started the recall
- FDA classified it Class I
- Published in FDA’s Enforcement Report
- FDA terminated the recall
Dates from the agency record only; steps without a date are left out.
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Where this comes from
The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
- Official source: FDA Recall #F-0097-2020 (October 1, 2019) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for F-0097-2020 to see it in context.
- Plain-language summary written by qwen3:4b on October 5, 2026, from the official record above. Not reviewed by a person — if it conflicts with the FDA notice, the notice is correct. Report an error on this page.
- GovInfoNow is an independent service and is not a government agency. We republish official FDA recall data; we don’t issue, amend or administer recalls.