4 Liter/6 Can Minifridges
Shaoxing ShangYu North Electron Manufacture Co. Ltd., of China
Summary
CPSC recall: 4 Liter/6 Can Minifridges. By Shaoxing ShangYu North Electron Manufacture Co. Ltd., of China. Hazard: The recalled minifridges' electrical switch can short circuit, posing fire and burn hazards.. Remedy: Consumers should immediately stop using the recalled minifridges and contact AstroAI for a free replacement minifridge. To receive a replacement minifridge, consumers should send a photo of the recalled minifridge, showing the model number and serial number, with "Recalled" written
Details
Source
CPSC Consumer Product Recall
External ID
10314
Action Date
2025-06-18
Status
Recalled
Category
consumer_product
Product Description
This recall involves the AstroAI 4-Liter/6-Can minifridges. AstroAI is printed on the front of the units. The model and
Context & Analysis
This is a unclassified recall.
This was one of 12 consumer_product recalls issued in the same week, part of 47 consumer_product-related FDA actions this month.
Shaoxing ShangYu North Electron Manufacture Co. Ltd., of China has 2 FDA actions in our database, including 1 recall.
Frequently Asked Questions
What is a FDA recall?
A Class III recall involves products that are unlikely to cause adverse health effects but violate FDA labeling or manufacturing regulations.
What should I do if I have this product?
Stop using the product. Check the product against the specific lot numbers or identifiers listed in the recall. Contact the manufacturer (Shaoxing ShangYu North Electron Manufacture Co. Ltd., of China) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.
How often does Shaoxing ShangYu North Electron Manufacture Co. Ltd., of China have FDA actions?
Shaoxing ShangYu North Electron Manufacture Co. Ltd., of China has 2 FDA actions in our database, including 1 recall and 0 device clearances.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "10314" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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