RecallHawk

Earthtec 7 3/8 Inch Pool Drain Covers

Shenzhen Qiangonghui Technology Co., Ltd., dba Tonyidea

Summary

CPSC recall: Earthtec 7 3/8 Inch Pool Drain Covers. By Shenzhen Qiangonghui Technology Co., Ltd., dba Tonyidea. Hazard: The recalled drain covers violate the entrapment protection standards of the Virginia Graeme Baker Pool and Spa Safety Act (VGBA), posing entrapment and drowning hazards to swimmers and bathers.. Remedy: Pool owners, pool operators and consumers should stop using pools with the recalled pool drain covers immediately. To receive a refund, consumers should remove the drain cover

Details

Source

CPSC Consumer Product Recall

External ID

10748

Action Date

2026-04-30

Status

Recalled

Category

consumer_product

Product Description

This recall involves Earthtec pool drain covers that are sold for use in swimming pools. The pool drain covers are 7 3/8

Context & Analysis

This is a unclassified recall.

This was one of 26 consumer_product recalls issued in the same week, part of 47 consumer_product-related FDA actions this month.

Shenzhen Qiangonghui Technology Co., Ltd., dba Tonyidea 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 Qiangonghui Technology Co., Ltd., dba Tonyidea) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.

How often does Shenzhen Qiangonghui Technology Co., Ltd., dba Tonyidea have FDA actions?

Shenzhen Qiangonghui Technology Co., Ltd., dba Tonyidea 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 "10748" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.

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