CLASS I Food recall · Reported 24 Jan 2018 · FDA Enforcement Report

Raspberry Cream Ice Cream Bars: Sundae Shoppe recalled

Fieldbrook Foods is recalling Raspberry Cream Ice Cream Bars: Sundae Shoppe, distributed nationwide in the US. The recall was initiated on 3 Jan 2018 and the FDA has classified it as Class I.

Check your package

Lot, batch or date codesThe recalled products have a production date of May 2017 to August 2017 and a best by date of May 2018 to August 2018.
Quantity recalled639,900 cases (total for all products)

Do not eat it. Return it to the store for a refund or throw it away. If you have symptoms after eating it, contact a doctor.

Recall details

Recall number
F-0686-2018
FDA event ID
78876
Recalling firm
Fieldbrook Foods, Dunkirk, NY
Classification
Class I
Status
Terminated
Recall initiated
3 Jan 2018
FDA classified
30 Jan 2018
Reported
24 Jan 2018
Type
Voluntary: Firm initiated
Customers notified by
Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit
Reason category
Listeria

Timeline

3 Jan 2018Recall initiated by company
24 Jan 2018Published in enforcement report+21 days
30 Jan 2018Classified by FDA+6 days

Companies usually start a recall weeks before the FDA classifies and publishes it; the gap above is that lag.

Reason for recall

Product may be contaminated with Listeria monocytogenes.

Listeria monocytogenes can grow at refrigerator temperatures. Infection is most dangerous for pregnant women, newborns, older adults and people with weakened immune systems. Symptoms can appear up to 70 days after eating contaminated food.

Product as listed by the FDA

RASPBERRY Cream Ice Cream Bars: Sundae SHOPPE, 12 Bars, UPC 041498204631

Where it was distributed

Sold to distributors in: MA, IL, CA, PR, CA, FL, MN, IL, OH, CT, MI, MO. Product was distributed nationwide including Puerto Rico.

Nationwide CaliforniaConnecticutFloridaIllinoisMassachusettsMichiganMinnesotaMissouriOhioPuerto Rico

Questions about this recall

Why was it recalled?

Product may be contaminated with Listeria monocytogenes.

Which lots are affected?

The recalled products have a production date of May 2017 to August 2017 and a best by date of May 2018 to August 2018.

Where was it sold?

Sold to distributors in: MA, IL, CA, PR, CA, FL, MN, IL, OH, CT, MI, MO. Product was distributed nationwide including Puerto Rico.

What should I do if I have it?

Do not eat it. Return it to the store for a refund or throw it away. If you have symptoms after eating it, contact a doctor.

What does Class I mean?

Class I is the most serious FDA recall category: there is a reasonable probability that using the product will cause serious health consequences or death.

Read the official FDA notice · Source record retrieved 26 Sep 2026. The FDA describes openFDA data as unvalidated; the official notice takes precedence. This page reports the record and gives no medical advice.

Other products in this recall event

3 other products · FDA event 78876

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