Unity 7 Shot 200 Gram Aerial Cake Firework Devices
Summary
CPSC recall: Unity 7 Shot 200 Gram Aerial Cake Firework Devices. By Pyro City stores, and other independent fireworks stores nationwide from January 2026 through May 2026 for between $6 and $8.. Hazard: The recalled fireworks can tip over, posing a risk of serious injury from explosion and burn hazards.. Remedy: Consumers should stop using the recalled fireworks immediately and return the fireworks to the store where they were purchased for a full refund. Consumers will receive the refund in the
Details
Source
CPSC Consumer Product Recall
External ID
10851
Action Date
2026-07-02
Status
Recalled
Category
consumer_product
Product Description
This recall involves the Unity 7 Shot 200 Gram Aerial Cake firework devices, model MEF6096. The recalled products were s
Context & Analysis
This is a unclassified recall.
This was one of 22 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 (Pyro City stores, and other independent fireworks stores nationwide from January 2026 through May 2026 for between $6 and $8.) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.
How often does Pyro City stores, and other independent fireworks stores nationwide from January 2026 through May 2026 for between $6 and $8. have FDA actions?
This is the only FDA action we have on record for Pyro City stores, and other independent fireworks stores nationwide from January 2026 through May 2026 for between $6 and $8. in our database.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "10851" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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