Sloosh Dive Sticks
Summary
CPSC recalled Sloosh Dive Sticks by Unknown Manufacturer. Hazard: The recalled dive sticks violate the federal dive sticks ban because they exceeded the compress limit, posing an impalement hazard. In shallow water, children may fall or land on a dive stick, resulting in serious piercing injuries. Facial and eye injuries are also possible when children attempt to retrieve the sticks underwater.. Remedy: Consumers should stop using the recalled dive sticks immediately, take them away from children and dispose of them. Consumers will be asked to take a photo of the disposed dive sticks in the trash and email it to Joyin at support@joyin.com. Once received, Joyin will send the consumer redesigned dive sticks that meet federal regulations..
Details
Source
cpsc
External ID
26536
Action Date
2026-06-11
Status
Ongoing
Category
product
Product Description
This recall involves Sloosh dive sticks, contained in packages of Sloosh water toys, model 40041. The model number 40041 is printed on the back of the box of Sloosh water toys, next to the bar code and printed on top of one end of the dive stick, along with Joyin's name and tracking information. The Sloosh water toys package contains 30 pieces, including five dive sticks. The recalled dive sticks are made of hard plastic and are cylinder-shaped. Each stick measures approximately 7-inches in length and about 1-inch or less in diameter. They come in various colors and are packaged in a box with other pool diving toys in the Sloosh water toys package. Only the dive sticks with model 40041 contained in the Sloosh water toys sold prior to October 23, 2025, are being recalled. Consumers can continue to use the other items contained in the Sloosh water toys package.
Company
Context & Analysis
Unknown Manufacturer has 1320 FDA actions in our database.
Frequently Asked Questions
How often does Unknown Manufacturer have FDA actions?
Unknown Manufacturer has 1320 FDA actions in our database, including 0 recalls 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.
Want to know the moment something like this happens?
Get alerts for productRelated Actions
American Angler Electric Fillet Knives
Weihai Yuanji Outdoor Products Co., Ltd. (RTI), of China · 2021-12-29
Polaris RZR and GENERAL Recreational Off-Road Vehicles
Unknown Manufacturer · 2021-12-23
The Captain Hang-on Treestands (2021 Batch #2M-0121)
Unknown Manufacturer · 2021-12-22
Carex Brand Adult Portable Bed Rails
Unknown Manufacturer · 2021-12-22
Endurance® Hand Bed Rails
Unknown Manufacturer · 2021-12-22