Jamba Juice brand Chunky Strawberry Topper
Reason The products were manufactured using peanut butter recalled by Sunland Inc. because it may be contaminated with Salmonella.
Jamba Juice brand Peanut Butter Moo'd Smoothie recall
Recalled by Jamba Juice · Emeryville, CA, United States
Class I — High risk. Reasonable probability of serious harm or death.
Why it was recalled
The products were manufactured using peanut butter recalled by Sunland Inc. because it may 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
Jamba Juice brand Peanut Butter Moo'd Smoothie; All sizes (small, medium, large); A Blend Of: Nonfat Vanilla Yogurt (Contains Milk), Chocolate Moo'd Base (Contains Milk), Soymilk (Contains Soy), Ice, Bananas, Peanut Butter (Contains Peanuts); The product is processed and packaged by Jamba Juice Co.
Quantity: Unknown
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.
No codes (Stop sale date: September 24, 2012)
Where it was sold
FDA's distribution note: Products were released for distribution in US.
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
- Jamba Juice
- Initiated by
- Voluntary: Firm initiated
- Recall initiated
- Sep 24, 2012
- In FDA report of
- Nov 14, 2012
- Terminated
- Dec 7, 2012
- FDA recall number
- F-0636-2013 · event 63346
- 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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