RecallHawk

Paddles sold with stand-up paddleboards

Agit Global Inc., of Taiwan

Summary

CPSC recalled Paddles sold with stand-up paddleboards by Agit Global Inc., of Taiwan. Hazard: The paddle can suddenly break mid-shaft into two pieces during use, exposing sharp edges and posing a risk of serious injury including puncture or laceration hazards.. Remedy: Consumers should immediately stop using the recalled paddles and contact Agit Global North America for a free, approximately two-foot long zippered paddle shaft sleeve, intended to be installed over the paddle shaft when the paddle is used..

Details

Source

cpsc

External ID

22210

Action Date

2022-08-25

Status

Ongoing

Category

product

Product Description

This recall involves Agit Global paddles, model years 2015 through 2020, that were sold with the 8', 8'6", 9'6", and 10'6" Wave Storm, Storm Blade, Ozoboard, True Wave, Bloo Tide, Dorsal, and Rock It Surf Stand-up paddleboards. The paddles are made of aluminum and are adjustable, between 5 and 7 feet in length. The paddles were provided with original purchase or as a replacement paddle under warranty and were not sold individually. Each paddle is printed with a four- or five-character manufacturing code on the paddle blade with one of the following prefixes or codes: Model Year Initial Characters of Manufacturing Code 2015 9'6 Wave Storm J4 2015 10'6" Wave Storm D5 2015 9'6" Dorsal B4, J4 2015 8'6", 9'6", 10'6" Ozoboards H4, F5 2015, 2016, and 2017 9'6" and 10'6" Storm Blades E5, F5, L5, B6, C6, B7, D7, E7, F7, G7 2016 9'6" Wave Storm I5, A6 2017 9'6" Wave Storm I6, L6, A7 2018 9'6" Wave Storm I7, K7 2018 9'6" Rock-It-Surf L8 2018 8' True Wave E8 2019 9'6" Wave Storm I8, K8, J901, J902, J903, J904 2019 8' Wave Storm L8 2019 9'6" Bloo Tide C9 2020 8' Wave Storm D0

Context & Analysis

Agit Global Inc., of Taiwan has 2 FDA actions in our database, including 1 recall.

Frequently Asked Questions

How often does Agit Global Inc., of Taiwan have FDA actions?

Agit Global Inc., of Taiwan 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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