So Delicious Dairy Free Salted Caramel Cluster Cashewmilk
Reason Product may contain foreign material: small stones and other hard objects.
Goldenbrook Farms Peanut Butter Bash Ice Cream recall
Recalled by Brookshire Grocery Company Manufacturing · Tyler, TX, United States
Class I — High risk. Reasonable probability of serious harm or death.
Why it was recalled
The product has the potential to be contaminated with Salmonella. The peanut butter used in the manufacturing of the ice cream was supplied by Sunland, Inc.
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
Goldenbrook Farms Peanut Butter Bash Ice Cream, 1/2 gallon carton with UPC code 0009282530538
Quantity: N/A
Food: Ice cream Peanut butter
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 Peanut Butter Bash Ice Cream distributed between May 2010 and September 2012 with UPC code 0009282530538.
Where it was sold
Arkansas Louisiana Texas
FDA's distribution note: TX, Louisiana and Southern Arkansas
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
- Brookshire Grocery Company Manufacturing
- Initiated by
- Voluntary: Firm initiated
- Recall initiated
- Oct 8, 2012
- In FDA report of
- May 29, 2013
- Terminated
- Jun 19, 2013
- FDA recall number
- F-1442-2013 · event 63418
- Official record
- FDA enforcement report search
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