RecallHawk

Body Glove Tandem Inflatable Stand Up Paddle Board, ULI Inventor Inflatable Paddle Board, ULI Zettian Inflatable Supyak

Jiangxi Aike Outdoor Sports, of China

Summary

CPSC recall: Body Glove Tandem Inflatable Stand Up Paddle Board, ULI Inventor Inflatable Paddle Board, ULI Zettian Inflatable Supyak and ULI Lila Inflatable Supyak. By Jiangxi Aike Outdoor Sports, of China. Hazard: The glue on the inflatable paddle boards can separate at the seams and the paddle boards can deflate unexpectedly, posing a drowning hazard.. Remedy: Consumers should immediately stop using the recalled boards and return them to Costco for a full refund or contact Surf 9 for instructi

Details

Source

CPSC Consumer Product Recall

External ID

9488

Action Date

2022-12-29

Status

Recalled

Category

consumer_product

Product Description

This recall involves the following: Body Glove Tandem Inflatable Stand Up Paddle Boards, ULI Inventor Inflatable Paddle

Context & Analysis

This is a unclassified recall.

This was one of 9 consumer_product recalls issued in the same week, part of 47 consumer_product-related FDA actions this month.

Jiangxi Aike Outdoor Sports, 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 (Jiangxi Aike Outdoor Sports, 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 Jiangxi Aike Outdoor Sports, of China have FDA actions?

Jiangxi Aike Outdoor Sports, 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 "9488" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.

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