Strawberry Sorbet
Reason Villa Dolce Gelato is recalling Strawberry Gelato and Strawberry Sorbetto because they have the potential to be contaminated with hepatitis A virus.
Strawberry Gelato recall
Recalled by Dolce Dolci LLC dba Villa Dolce Gelato · Reseda, CA, United States
Class I — High risk. Reasonable probability of serious harm or death.
Why it was recalled
Villa Dolce Gelato is recalling Strawberry Gelato and Strawberry Sorbetto because they have the potential to be contaminated with hepatitis A virus.
Pathogen: Hepatitis A
A virus spread through contaminated produce and seafood.
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 Gelato, 5 Liter, 1 unit/case
Quantity: 602 units
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.
Exp. Date Feb 5, 2018 Exp. Date March 19, 2018
Where it was sold
Nationwide.
Arizona California Colorado Florida Illinois Massachusetts Maryland Minnesota Montana North Dakota Nevada New York Oklahoma South Carolina Utah
FDA's distribution note: Nationwide in US: OK, CA, NV, MD, CA, FL, MA, NY, CO, AZ, SC, MN, ND, UT, MT, IL
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. 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
- Dolce Dolci LLC dba Villa Dolce Gelato
- Initiated by
- Voluntary: Firm initiated
- Recall initiated
- Nov 30, 2016
- In FDA report of
- Mar 29, 2017
- Terminated
- May 1, 2017
- FDA recall number
- F-1692-2017 · event 75861
- Official record
- FDA enforcement report search
Also recalled with it (1 more product)
FDA files each product of one recall action separately; these share the same FDA event.
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