Cardboard box contain 6 paper packets each labeled as: Fresh Food Manufacturing Company Firecracker Burger Kit Keep Refrigerated Mix ...
⚠ Critical Alert — Stop Using Immediately
This product has been flagged with severe risks (fire or burn). Stop using it now and contact the brand or FDA for a refund, repair, or replacement.
FDA Recall Notice
Source: U.S. Food and Drug Administration (FDA) — official FDA notice for recall FDA-F-1225-2015.
Firm manufactured Firecracker Burger Kits utilizing Cumin, currently recalled by supplier. Kits were utilized by retail stores to manufacture Firecracker Salmon Burgers sold in-store only.
Corrective Action (per FDA)
Source: U.S. Food and Drug Administration (FDA) — official FDA notice for recall FDA-F-1225-2015.
Recall terminated by FDA.
✅ What you should do
- Stop using the product if you own it.
- Check the model number, lot code, or sell-by date against the recall notice above.
- Contact Fresh Foods Manufacturing Co. or the retailer where you bought it for a refund, replacement, or repair.
- For the most current official instructions, visit the FDA recall page.
- If you've been hurt by this product, report the incident to FDA.
Consumer Contact (per FDA)
Source: U.S. Food and Drug Administration (FDA) — official FDA notice for recall FDA-F-1225-2015.
Fresh Foods Manufacturing Co.
About the U.S. Food and Drug Administration
The FDA regulates drugs, medical devices, food, cosmetics, and tobacco. Adverse event reports and recall notices are the main public safety signal.
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If you had a reaction, found contamination, or experienced a labeling problem with this product, report it to the FDA. The agency uses consumer reports to track emerging safety signals and trigger recalls.
Fresh Foods Manufacturing Co. Recall FAQ
Fresh Foods Manufacturing Co. is the subject of a bakery & grains safety report: Cardboard box contain 6 paper packets each labeled as: Fresh Food Manufacturing Company Firecracker Burger Kit Keep Refrigerated Mix .... The notice was published on January 16, 2015 by the U.S. Food and Drug Administration (FDA). Approximately 15 units are potentially affected.