RecallHawk

Summary

CPSC recall: Supernova and Typhoon Lighters. By Small independent stores nationwide and online at prestigeimportgroup.com from October 2023 through March 2026 for between $7 and $10.. Hazard: The recalled lighters violate the mandatory standard for cigarette lighters because they do not have the required child-resistant mechanism, posing a risk of serious injury or death from fire and burn hazards. In addition, the lighters failed to meet the pre-market lighter submission requirement needed to d

Details

Source

CPSC Consumer Product Recall

External ID

10709

Action Date

2026-04-09

Status

Recalled

Category

consumer_product

Product Description

This recall involves two Prestige-branded metal butane torch lighters. The Supernova gray and black lighters have a rugg

Context & Analysis

This is a unclassified recall.

This was one of 30 consumer_product recalls issued in the same week, part of 47 consumer_product-related FDA actions this month.

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 (Small independent stores nationwide and online at prestigeimportgroup.com from October 2023 through March 2026 for between $7 and $10.) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.

How often does Small independent stores nationwide and online at prestigeimportgroup.com from October 2023 through March 2026 for between $7 and $10. have FDA actions?

This is the only FDA action we have on record for Small independent stores nationwide and online at prestigeimportgroup.com from October 2023 through March 2026 for between $7 and $10. in our database.

Where can I find the official FDA record?

The official record is available on FDA.gov. Search for "10709" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.

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