GANCHI NAIWEITANGPIAN Candy NET WT: 280G(9.8oz) in cardboard package. 24 packages per master case. The following codes are listed on the individual packages: 20190316 (stamped on box), BEST BEFORE: 03.15.2020, UPC 6926106100083. INGREDIENTS: sugar, glucose, planting the fat end, (glucose syrup, soybean oil, shortening, casein acid sodium, span 60, FD&C Yellow 5). RONG SHING TRADING NY INC. 47-57 BRIDGEWATER STREET BROOKLYN NY 11222.
Reported: November 6, 2019 Initiated: September 26, 2019 #F-0091-2020
Product Description
GANCHI NAIWEITANGPIAN Candy NET WT: 280G(9.8oz) in cardboard package. 24 packages per master case. The following codes are listed on the individual packages: 20190316 (stamped on box), BEST BEFORE: 03.15.2020, UPC 6926106100083. INGREDIENTS: sugar, glucose, planting the fat end, (glucose syrup, soybean oil, shortening, casein acid sodium, span 60, FD&C Yellow 5). RONG SHING TRADING NY INC. 47-57 BRIDGEWATER STREET BROOKLYN NY 11222.
Reason for Recall
Product contains undeclared milk
Details
- Recalling Firm
- Rong Shing Trading Inc.
- Units Affected
- 54 cartons; 24 packages/carton; Total: 1,296 packages
- Distribution
- Retailer in 7 states: KY, MD, NY, UT, VA, VT, and WA.
- Location
- Brooklyn, NY
Frequently Asked Questions
What product was recalled? ▼
GANCHI NAIWEITANGPIAN Candy NET WT: 280G(9.8oz) in cardboard package. 24 packages per master case. The following codes are listed on the individual packages: 20190316 (stamped on box), BEST BEFORE: 03.15.2020, UPC 6926106100083. INGREDIENTS: sugar, glucose, planting the fat end, (glucose syrup, soybean oil, shortening, casein acid sodium, span 60, FD&C Yellow 5). RONG SHING TRADING NY INC. 47-57 BRIDGEWATER STREET BROOKLYN NY 11222.. Recalled by Rong Shing Trading Inc.. Units affected: 54 cartons; 24 packages/carton; Total: 1,296 packages.
Why was this product recalled? ▼
Product contains undeclared milk
Which agency issued this recall? ▼
This recall was issued by the FDA Food on November 6, 2019. Severity: Moderate. Recall number: F-0091-2020.
Related Recalls
FDA Devices Moderate
Convenience Kits 1. 25GA Convenience Kit - FNX VS0644.25-FNX 2. 25GA Convenience Kit - FXX VS0644.25-FXX 3.2…
Vortex Surgical Inc. · 2026-02-11
FDA Devices Moderate
COULTER DxH Diluent, REF 628017 COULTER DxH ECO Diluent REF C67250 For use as an isotonic buffered diluent in conju…
Beckman Coulter, Inc. · 2026-02-11
FDA Devices Moderate
Product Name: Single Use 3-Lumen Sphincterotome V Model/Catalog Number: KD-V411M-1520 Product Description: These inst…
Olympus Corporation of the Americas · 2026-02-11
FDA Devices Moderate
Product Name: Disposable Triple Lumen Sphincterotome Model/Catalog Number: KD-401Q-0330 Product Description: These in…
Olympus Corporation of the Americas · 2026-02-11
FDA Devices Moderate
Product Name: Lumipulse pTau 217 Plasma Controls Model/Catalog Number: 81558 Software Version: Not Applicable Produc…
Fujirebio Diagnostics, Inc. · 2026-02-11