Food Recall Check
Class I · High risk Ongoing Initiated Oct 5, 2018 (8 years ago)

Ladyfingers Gourmet to Go Signature Shaved Country Ham Rolls recall

Recalled by Ladyfingers Catering, LLC · Raleigh, NC, United States

Class I — High risk. Reasonable probability of serious harm or death.

Why it was recalled

The firm was notified by their vendor that the product may be contaminated with Listeria monocytogenes.

Pathogen: Listeria

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

LADYFINGERS GOURMET TO GO SIGNATURE SHAVED COUNTRY HAM ROLLS; ONE DOZEN PER PACKAGE (15oz - 425 grams); ALLERGEN INFORMATION: CONTAINS WHEAT, PRODUCED IN FACILITY THAT PROCESSES PEANUTS AND TREE NUTS. www.ladyfingersofraleigh.com; 919-828-2270; 627 East Whitaker Mill Rd Raleigh, NC 27608; UPC 8 56149 00509 9.

Quantity: 50,627 packages

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.

All product on the market.

Where it was sold

California District of Columbia Delaware Georgia North Carolina New York South Carolina Virginia

FDA's distribution note: Product was shipped to the following states: CA, DE, GA, NC, NY, SC, VA & DC.

Do not eat it. Class I means FDA judged there is a reasonable probability of serious illness or death. If the brand, size and lot or date code on your package match, throw the product away or return it to the store for a refund, and clean any surface or container it touched. If anyone has eaten it and feels unwell, contact a doctor and mention the recall.

Recalling firm
Ladyfingers Catering, LLC
Initiated by
Voluntary: Firm initiated
Recall initiated
Oct 5, 2018
In FDA report of
Oct 31, 2018
FDA recall number
F-0065-2019 · event 81175
Official record
FDA enforcement report search