Strawberry Shortcake Bar recall

Recalled by Rich Ice Cream Co · West Palm Beach, FL, United States

Class II — Moderate risk. May cause temporary or reversible harm; serious harm unlikely.

Why it was recalled

Potential Listeria Monocytogenes Contamination

Listeria monocytogenes can grow even in the fridge and is especially dangerous in pregnancy.

The most serious food recalls: a contaminated product can cause outbreaks, hospitalisations and deaths, especially for pregnant people, young children, older adults and anyone with a weakened immune system. All bacteria & viruses recalls.

What was recalled

Strawberry Shortcake Bar (85050), stick novelties 3 FL. Oz (89mL)., Individually packaged in a plastic bag. Master case that consists of 4 packers with 24 units in each packer, total 96 units in a master case. Keep Frozen.

Quantity: Total of 110,292 cases to include all products

Food: Berries

Lot codes, dates and UPCs

A recall covers only these codes. Compare them with the lot number, best-by date or UPC printed on your package.

Lot # 24351 through lot # 25156 (Julian calendar)

Where it was sold

Alabama Arizona California Florida Georgia Iowa Illinois Louisiana Massachusetts Missouri Nebraska New Jersey Nevada New York Ohio Oklahoma Oregon Pennsylvania South Carolina Tennessee Texas Virginia Wisconsin

FDA's distribution note: Distributed to: CA, PA, OH, GA, NY, NJ, FL, TX, VA, AZ, AL, IL, MO, MA, TN, IA, SC, OR, OK, NV, LA, WI, NE, Nassau, Bahamas

Check the codes, then return or discard. Class II means eating it may cause temporary or reversible health problems. If your package matches the recalled codes, do not eat it - return it to the store or throw it away. FDA lists this recall as terminated: the company has finished removing the product, so it should no longer be on shelves - but it can still be in a freezer or pantry.

Recalling firm: Rich Ice Cream Co
Initiated by: Voluntary: Firm initiated
Recall initiated: Jun 27, 2025
In FDA report of: Jul 23, 2025
Terminated: Jan 21, 2026
FDA recall number: H-0285-2025 · event 97163
Official record: FDA enforcement report search