SEGMART 55" Indoor/Outdoor Mini Round Toddler Trampolines with Enclosure Nets and Accessory Kits
Summary
CPSC recall: SEGMART 55" Indoor/Outdoor Mini Round Toddler Trampolines with Enclosure Nets and Accessory Kits. By Shenzhen Segmart Technology Electronics Co., Ltd., of China. Hazard: Young children can become entangled in the straps of the hammock, punching bag and hand ring accessories, posing a strangulation hazard, which can result in serious injury or death.. Remedy: Consumers should remove the hammock, punching bag, hand ring and basketball board accessories immediately before continuing to
Details
Source
CPSC Consumer Product Recall
External ID
10718
Action Date
2026-04-16
Status
Recalled
Category
consumer_product
Product Description
This recall involves SEGMART 55" indoor/outdoor mini round toddler trampolines with enclosure nets. Certain versions of
Context & Analysis
This is a unclassified recall.
This was one of 37 consumer_product recalls issued in the same week, part of 47 consumer_product-related FDA actions this month.
Shenzhen Segmart Technology Electronics 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 (Shenzhen Segmart Technology Electronics 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 Shenzhen Segmart Technology Electronics Co., Ltd., of China have FDA actions?
Shenzhen Segmart Technology Electronics 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 "10718" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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