RecallHawk

Bright Builder Fort Kits with Flashlights

Unknown Manufacturer

Summary

CPSC recalled Bright Builder Fort Kits with Flashlights by Unknown Manufacturer. Hazard: The flashlight on the recalled kits violates the mandatory federal battery-operated toy regulation because the flashlights contain button cell batteries in a compartment that can be easily opened without requiring the use of a common household tool. When button cell batteries are swallowed, the ingested batteries can cause serious injuries, internal chemical burns, and death, posing an ingestion hazard.. Remedy: Consumers should immediately stop using the flashlights in the recalled fort kits, keep them away from children, and contact Intellio Toys for instructions on how to receive a refund between $10 and $15, depending on the model. Consumers can continue to use the fort kits without the flashlights. Button cell batteries are hazardous. Batteries should be disposed of or recycled by following local procedures for hazardous household waste. Amazon and Intellio Toys are contacting all known purchasers directly..

Details

Source

cpsc

External ID

24363

Action Date

2024-09-12

Status

Ongoing

Category

product

Product Description

This recall involves Intellio Toys' Bright Builder fort kits, models FKL-BG, FKL-BR, L-5BG and L-5BR. The green and blue, or red and blue, 100-piece fort-building kits contain 45 long sticks, 25 short sticks, 15 connecting tubes, 25 multilink balls, and a pack of five flashlights with button cell batteries. The flashlights were sold as part of the kit and individually as an add add-on component. "Bright Builder" is on the front of the kit box and "Intellio Toys" is on the side panel. The model number can be found on the bottom right corner of the back of the box. Only Bright Builder fort kits with flashlights are included in this recall.

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.

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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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