RecallHawk

Evajoy 48-inch and taller above-ground pools

Shenzhen Danya Tech Co., Ltd. d/b/a Evajoy, of China

Summary

CPSC recall: 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 child

Details

Source

CPSC Consumer Product Recall

External ID

10651

Action Date

2026-02-26

Status

Recalled

Category

consumer_product

Product Description

This recall involves all Evajoy above-ground pools 48 inches and taller. Models EJ-HF032, EJ-HF044, and EJ-HF045 are inc

Context & Analysis

This is a unclassified recall.

This was one of 35 consumer_product recalls issued in the same week, part of 47 consumer_product-related FDA actions this month.

Shenzhen Danya Tech Co., Ltd. d/b/a Evajoy, 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 Danya Tech Co., Ltd. d/b/a Evajoy, 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 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. Search for "10651" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.

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