RecallHawk

Ceramic Pulley for Switchblade and Drifter kite sailing kites

Unknown Manufacturer

Summary

CPSC recalled Ceramic Pulley for Switchblade and Drifter kite sailing kites by Unknown Manufacturer. Hazard: The ceramic pulleys used in the recalled Switchblade and Drifter kiteboarding kites can cause the bridle line connection to break, which reduces performance in steering and control of the kite, causing the kiteboarder to lose control of the kite, posing an injury hazard.. Remedy: Consumers should immediately stop using the recalled Switchblade and Drifter kite sailing kites and contact the place where purchased, an authorized dealer or Adventure Sports for a free replacement kit with installation instructions for the kites. Consumers will receive a replacement kit to make the repair, or can request vendor assistance to replace the pulley. The firm is contacting all known purchasers directly regarding the recall..

Details

Source

cpsc

External ID

22764

Action Date

2022-07-28

Status

Ongoing

Category

product

Product Description

This recall involves two (2) white ceramic pulleys, with the marking Cabrinha on each of the pulleys, on the Cabrinha® Switchblade and Drifter Kites for kite surfing with model number 02 and serial numbers beginning with one of the following: 61NI, 61NJ, 61NK, 61NL, 62NA, 62NB, 62NC, C11G, C11H, C11K. The model and serial numbers are on the outer box containing the kites, on the hangtags of the kites and on the trailing edge of the kite's label. The packaging for the kites does not have a green dot on the hangtag and outer shipping box. The recall includes two white ring ceramic pieces/guides (two per kite).

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 product

Related Actions