Frigidaire-brand Minifridges, models EFMIS129, EFMIS137, EFMIS149 and EFMIS175, limited to the listed serial numbers
Summary
CPSC recall: Frigidaire-brand Minifridges, models EFMIS129, EFMIS137, EFMIS149 and EFMIS175, limited to the listed serial numbers. By ShangYu North Electron Manufacture Co. Ltd., of China. Hazard: The minifridges' internal electrical components can short circuit and ignite the surrounding plastic housing, posing fire and burn hazards.. Remedy: Consumers should immediately stop using the recalled minifridges and follow the instructions to receive a refund at www.recallrtr.com/minifridge. Consumer
Details
Source
CPSC Consumer Product Recall
External ID
10352
Action Date
2025-07-24
Status
Recalled
Category
consumer_product
Product Description
This recall involves Curtis International minifridges. "Frigidaire" is printed on the front of the units. The model and
Context & Analysis
This is a unclassified recall.
This was one of 20 consumer_product recalls issued in the same week, part of 47 consumer_product-related FDA actions this month.
ShangYu North Electron Manufacture Co. Ltd., of China has 4 FDA actions in our database, including 2 recalls.
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 (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 ShangYu North Electron Manufacture Co. Ltd., of China have FDA actions?
ShangYu North Electron Manufacture Co. Ltd., of China has 4 FDA actions in our database, including 2 recalls and 0 device clearances.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "10352" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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