Evajoy 48-inch and taller above-ground pools
Summary
CPSC recalled Evajoy 48-inch and taller above-ground pools by Shenzhen Danya Tech Co., Ltd. d/b/a Evajoy, of China. Hazard: The compression strap that surrounds the outside of the pool legs may create a foothold, allowing a child access to the pool, posing a drowning risk.. Remedy: Consumers should contact Evajoy to request a free repair kit that removes the compression strap from the pool, while maintaining the structural integrity of the pool. In the interim, consumers should ensure that children cannot access the pool unattended or, alternatively, drain the pool until the repair can be installed..
Details
Source
cpsc
External ID
26308
Action Date
2026-02-26
Status
Ongoing
Category
product
Product Description
This recall involves all Evajoy above-ground pools 48 inches and taller. Models EJ-HF032, EJ-HF044, and EJ-HF045 are included in this recall. Model EJ-HF032 measures 16 feet in diameter by 48 inches in height. Model EJ-HF044 measures 18 feet in diameter by 52 inches in height. Model EJ-HF045 measures 24 feet in diameter by 52 inches in height. Model information and the Evajoy logo are printed on the liner on the outside of the pool. The recalled above-ground pools contain a compression strap (also referred to as a reinforcing belt) that wraps around the pool on the outside of the vertical support poles, and may create a foothold, allowing a child to access the pool and drown. Children can still gain access to the pools using these footholds even if the ladder is removed. CPSC's website www.PoolSafely.gov has free, downloadable educational materials available to the public on pool safety including information on barriers, covers, alarms and other safety information.
Context & Analysis
Shenzhen Danya Tech Co., Ltd. d/b/a Evajoy, of China has 2 FDA actions in our database, including 1 recall.
Frequently Asked Questions
How often does Shenzhen Danya Tech Co., Ltd. d/b/a Evajoy, of China have FDA actions?
Shenzhen Danya Tech Co., Ltd. d/b/a Evajoy, 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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