Dark Chocolate Dolcini
Reason Dark Chocolate Dolcini and Limoncello Dolcini were made using ingredients which was allegedly affected by the dry milk recall from Valley Milk and could potentially be contaminated with Salmonella.
Limoncello Dolcini In clear plastic cup recall
Recalled by Steven Roberts Originals, LLC · Denver, CO, United States
Class I — High risk. Reasonable probability of serious harm or death.
Why it was recalled
Dark Chocolate Dolcini and Limoncello Dolcini were made using ingredients which was allegedly affected by the dry milk recall from Valley Milk and could potentially be contaminated with Salmonella.
Pathogen: Salmonella
Salmonella is the most common cause of food recalls for bacteria, often in eggs, produce, nuts and spices.
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
Limoncello Dolcini , In clear plastic cup, 72 individual servings, Store frozen
Quantity: 145 cases
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 No.: 338-16C2
Where it was sold
California Colorado Texas Virginia
FDA's distribution note: California, Texas and Colorado. No foreign/VA/govt/military
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
- Steven Roberts Originals, LLC
- Initiated by
- Voluntary: Firm initiated
- Recall initiated
- Dec 9, 2016
- In FDA report of
- Jan 25, 2017
- Terminated
- Jul 5, 2017
- FDA recall number
- F-1231-2017 · event 75967
- 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.