RecallHawk

Purefog High Density Natural Fog Juice Liquids

Pure Brands of California, of San Diego, California

Summary

CPSC recall: Purefog High Density Natural Fog Juice Liquids. By Pure Brands of California, of San Diego, California. Hazard: The recalled fog liquid can expire sooner than the expiration date listed on the product. This can pose a risk of respiratory or other infections in individuals with compromised immune systems, damaged lungs or an allergy to mold.. Remedy: Consumers should immediately stop using the recalled product, discard the unused product by pouring it down the drain, and contact the

Details

Source

CPSC Consumer Product Recall

External ID

9903

Action Date

2024-03-28

Status

Recalled

Category

consumer_product

Product Description

This recall involves Purefog High Density Natural Fog Juice Liquid, Long Lasting, Water Based for all Fog Machines 400-1

Context & Analysis

This is a unclassified recall.

This was one of 12 consumer_product recalls issued in the same week, part of 47 consumer_product-related FDA actions this month.

Pure Brands of California, of San Diego, California has 2 FDA actions in our database, including 1 recall.

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 (Pure Brands of California, of San Diego, California) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.

How often does Pure Brands of California, of San Diego, California have FDA actions?

Pure Brands of California, of San Diego, California has 2 FDA actions in our database, including 1 recall and 0 device clearances.

Where can I find the official FDA record?

The official record is available on FDA.gov. Search for "9903" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.

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