CLASS I Food recall · Reported 15 Apr 2015 · FDA Enforcement Report

Talenti Gelato & Sorbetto, 1 pt. with best by date 5/19/2016 recalled

Unilever United States is recalling Talenti Gelato & Sorbetto, 1 pt. with best by date 5/19/2016, distributed nationwide in the US. The recall was initiated on 27 Feb 2015 and the FDA has classified it as Class I.

Check your package

Lot, batch or date codesBest by date 5/19/2016

Quantity recalled5,810 cases

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-1923-2015
FDA event ID: 70629
Recalling firm: Unilever United States, Englewood Cliffs, NJ
Brand: Talenti Gelato
Classification: Class I
Status: Terminated
Recall initiated: 27 Feb 2015
FDA classified: 7 Apr 2015
Reported: 15 Apr 2015
Type: Voluntary: Firm initiated
Customers notified by: Press Release
Reason category: Undeclared Peanuts
Product category: Ice Cream & Frozen Desserts

Timeline

27 Feb 2015	Recall initiated by company
7 Apr 2015	Classified by FDA	+39 days
15 Apr 2015	Published in enforcement report	+8 days

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

Reason for recall

Talenti Gelato & Sorbetto, a Unilever Company is voluntarily recalling a limited number of jars of Talenti Gelato & Sorbetto Sea Salt Carmel Gelato because they may inadvertently contain peanuts (as peanut butter) which are not listed as an ingredient on the label.

Product as listed by the FDA

Talenti Gelato & Sorbetto, 1 pt. (473 mL) in clear plastic jars with best by date 5/19/2016, UPC 8685200024

Where it was distributed

US Nationwide

Nationwide

Questions about this recall

Why was it recalled?

Which lots are affected?

Best by date 5/19/2016

Where was it sold?

US Nationwide

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.

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