Recall Ledger

Lava Bun with Salted Egg Yolk orange packaging recall (Prime Food Processing LLC.)

FoodClass IITerminated

Summary: Prime Food Processing LLC. is recalling Lava Bun with Salted Egg Yolk orange packaging (Frozen) Unsalted butter and cream are listed in the ingredient statement.. Reason: Products do not declare milk in the Contains statement or the ingredient statement.

What is being recalled

Lava Bun with Salted Egg Yolk orange packaging (Frozen) Unsalted butter and cream are listed in the ingredient statement.

Why

Products do not declare milk in the Contains statement or the ingredient statement.

How serious is it

Class II is the middle level: using or being exposed to this product may cause temporary or medically reversible health problems, and the chance of serious harm is remote.

Where it was sold

AL, AZ, CA, CO, CT, FL, GA, HI, IL, IN, KS, LA, MA, MD, ME, MI, MO, MS, NC, NE, NJ, NY, OH, OK, OR, PA, RI, TN, TX, UT, VA, WA, WI (states named: Alabama, Arizona, California, Colorado, Connecticut, Florida, Georgia, Hawaii, Illinois, Indiana, Kansas, Louisiana, Massachusetts, Maryland, Maine, Michigan, Missouri, Mississippi, North Carolina, Nebraska, New Jersey, New York, Ohio, Oklahoma, Oregon, Pennsylvania, Rhode Island, Tennessee, Texas, Utah, Virginia, Washington, Wisconsin)

How to tell if yours is affected

all production dates between April 2-November 14, 2025.

What to do

Check the product name and the codes above against what you have. If they match, do not eat or use it. Throw it away or return it to the store where you bought it, and contact the recalling company with questions.

Recall facts

Recall numberH-0230-2026
CategoryFood
AgencyU.S. Food and Drug Administration (FDA)
SeverityClass II
StatusTerminated
Recall startedNovember 16, 2025
ReportedDecember 10, 2025
CompanyPrime Food Processing LLC.
Company locationBrooklyn, NY, United States
Initiated byVoluntary: Firm initiated
Quantity2,243 cases (total)

More recalls from Prime Food Processing LLC. · all food recalls · recalls from November 2025

Official FDA record