RecallHawk

Credhedz Lizard Helmets, Crayola Dry Erase Helmets and Tony Hawk Multi-Purpose Helmets

Sakar International Inc., of Edison, New Jersey

Summary

CPSC recall: Credhedz Lizard Helmets, Crayola Dry Erase Helmets and Tony Hawk Multi-Purpose Helmets. By Sakar International Inc., of Edison, New Jersey. Hazard: The recalled helmets do not comply with the positional stability and retention system requirements of the U.S. CPSC federal safety standard for bicycle helmets. The helmets can fail to protect in the event of a crash, posing a risk of head injury.. Remedy: Consumers should immediately stop using the recalled helmets and contact Sakar for

Details

Source

CPSC Consumer Product Recall

External ID

9505

Action Date

2023-01-19

Status

Recalled

Category

consumer_product

Product Description

This recall involves three helmet models from Sakar International; Tony Hawk, Credhedz Lizard and Crayola Dry-Erase helm

Context & Analysis

This is a unclassified recall.

This was one of 17 consumer_product recalls issued in the same week, part of 47 consumer_product-related FDA actions this month.

Sakar International Inc., of Edison, New Jersey has 6 FDA actions in our database, including 3 recalls.

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 (Sakar International Inc., of Edison, New Jersey) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.

How often does Sakar International Inc., of Edison, New Jersey have FDA actions?

Sakar International Inc., of Edison, New Jersey has 6 FDA actions in our database, including 3 recalls and 0 device clearances.

Where can I find the official FDA record?

The official record is available on FDA.gov. Search for "9505" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.

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