FDA Notice: Magic Gourmet Trading Inc Issues Nationwide Recall for Koi Palace Mini Moon Cake: Single Box - Mini Oolong Tea Past
Magic Gourmet Trading Inc has initiated a Class II recall affecting Koi Palace Mini Moon Cake: Single Box - Mini Oolong Tea Paste Unit Size 1/2 lb. and 1/4 lb. in circular box (1 piece) and rectangular boxes (4, 6 or due to Mooncake products, manufactured and distributed by Magic Gourmet Trading, Inc. of Milbrae, CA did not have adequate product labeling, including ingred.
A public safety recall has been officially logged by the U.S. Food and Drug Administration (FDA). Consumers in possession of the affected product in California are advised to stop use immediately and contact the manufacturer for a free remedy or refund.
“A public safety recall has been officially logged by the U.S. Food and Drug Administration (FDA). Consumers in possession of the affected product in California are advised to stop use immediately and contact the manufacturer for a free remedy or refund.”
Key Verified Points
- •Recalling Entity: Magic Gourmet Trading Inc
- •Product Description: Koi Palace Mini Moon Cake: Single Box - Mini Oolong Tea Paste Unit Size 1/2 lb. and 1/4 lb. in circular box (1 piece) and rectangular boxes (4, 6 or 8 pieces).
- •Recall Classification: Class II
- •Reason for Recall: Mooncake products, manufactured and distributed by Magic Gourmet Trading, Inc. of Milbrae, CA did not have adequate product labeling, including ingredient statements and allergen declaration. Undeclar
- •Distribution Footprint: CA, WA, OR.
- •FDA Status: Terminated
Public Safety & Consumer Recall Overview
Magic Gourmet Trading Inc has initiated a Class II recall affecting Koi Palace Mini Moon Cake: Single Box - Mini Oolong Tea Paste Unit Size 1/2 lb. and 1/4 lb. in circular box (1 piece) and rectangular boxes (4, 6 or due to Mooncake products, manufactured and distributed by Magic Gourmet Trading, Inc. of Milbrae, CA did not have adequate product labeling, including ingred.
Identified Hazard & Consumer Risk
Federal safety regulators and issuing authorities at the U.S. Food and Drug Administration (FDA) have documented consumer hazards associated with this product. The advisory carries an official urgency level of EXPECTED and severity classified as SEVERE.
Verified Product Specifications & Campaign Records
Geographic Distribution & Nationwide Scope
Consumer Remedy & Action Checklist
Regulatory Provenance
This bulletin is compiled directly from public safety filings logged by the U.S. Food and Drug Administration (FDA). For additional support or to report an adverse event, consult the official record at https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts.
Event Timeline & Developments
Frequently Asked Questions
What should consumers do if they own the recalled product?
Consumers should discontinue use immediately and follow the remedy instructions published by the U.S. Food and Drug Administration (FDA), which include free replacement, repair, or full refund.
Is there any cost to the consumer for recall remedies?
No. Under United States federal consumer protection laws, remedies, repairs, and safety replacements for officially recalled goods are provided free of charge.
Who is the primary federal authority overseeing this recall?
This action is monitored by the U.S. Food and Drug Administration (FDA) and logged in official federal public safety recall registries.
Official Government & Primary Citations
- U.S. Food and Drug Administration (FDA) — https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts
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