Class ITerminatedVoluntary: Firm initiated

Fabalish,: food recall F-0290-2025

Fabalish, of Carlstadt, NJ recalled Fabalish Inc. , Kickin, Carrot Falafel , 10oz , Cardboard tray inside plastic film inside cardboard box, individual… Reason: Potential E Coli contamination. The FDA listed it as Class I in its Enforcement Report dated Dec 25, 2024; distribution: California, Colorado, Florida, Georgia, Illinois, Indiana, Kansas, Massachusetts, Montana, Nebraska, New Hampshire, New York, Ohio, Tennessee, Texas, Utah, Virginia, Washington.

Record status as published: Terminated (terminated Jun 12, 2025). openFDA data last updated Oct 21, 2026.

Have this product? Check FDA.gov and your retailer. This page reproduces an FDA Enforcement Report record and is not a public alert. Look for the firm's recall notice on the FDA's recalls page, or ask the store where you bought it what to do. If you think you got sick from a food, contact a health care provider.

Recall details

Product
Fabalish Inc. , Kickin, Carrot Falafel , 10oz , Cardboard tray inside plastic film inside cardboard box, individual units
Product quantity
57 Units
Reason for recall
Potential E Coli contamination.
Codes, lots and dates on the package
Batch Lot: 240926 , Finished Good Lot: 260925 ,UPC: 850001779074,
Distribution pattern
CA, CO, FL, GA, IL, IN, KS, MA, MT, NE, NH, NY, OH, TN,TX, UT, VA, WA
Recalling firm
Fabalish,, Carlstadt, NJ
Classification
Class I — the FDA uses this class for a situation in which there is a reasonable probability that using or being exposed to the product will cause serious adverse health consequences or death.
Voluntary or mandated
Voluntary: Firm initiated
How the firm first notified customers
Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit

Dates

EventDate
Recall initiated by the firmNov 18, 2024
Classified by the FDADec 16, 2024
Published in the Enforcement ReportDec 25, 2024
TerminatedJun 12, 2025

All food recall records

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Sources

  • U.S. Food and Drug Administration, openFDA food enforcement reports, recall number F-0290-2025 (openFDA record). Data provided by the U.S. Food and Drug Administration (https://open.fda.gov).
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