RecallHawk

SEGMART 55" Indoor/Outdoor Mini Round Toddler Trampolines with Enclosure Nets and Accessory Kits

Shenzhen Segmart Technology Electronics Co., Ltd., of China

Summary

CPSC recalled 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 use the trampoline. SEGMART will provide a $30 refund to consumers who remove and destroy the hammock, punching bag, hand ring and basketball board accessories. Consumers will be asked to cut the straps on the accessories and submit photos of the cut accessories to the firm. Instructions can be found at www.segmart.com..

Details

Source

cpsc

External ID

26414

Action Date

2026-04-16

Status

Ongoing

Category

product

Product Description

This recall involves SEGMART 55" indoor/outdoor mini round toddler trampolines with enclosure nets. Certain versions of the trampolines included promotional accessory kits consisting of a hammock, punching bag, hand rings, basketball board, basketball, pump and colorful balls. The trampolines and accessories come in a variety of colors. Model numbers SOSTT051BR, SOSTT051CR and SOSTT051YP are included in the recall. The model number can be found on a label located on the handlebar of the trampoline. Trampolines that did not include promotional accessory kits are not included in the recall.

Context & Analysis

Shenzhen Segmart Technology Electronics Co., Ltd., of China has 2 FDA actions in our database, including 1 recall.

Frequently Asked Questions

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. Use the link above to view the complete official filing. You can also use the openFDA API to query this record programmatically.

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