Snow Monkey Subzero Superfood Cacao
Reason Potential Listeria monocytogenes contamination.
Snow Monkey Subzero Superfood Goji Berry recall
Recalled by FMIF Holdings, LLC dba Snow Monkey · Santa Monica, CA, United States
Class I — High risk. Reasonable probability of serious harm or death.
Why it was recalled
Potential Listeria monocytogenes contamination.
Pathogen: Listeria
Listeria monocytogenes can grow even in the fridge and is especially dangerous in pregnancy.
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
Snow Monkey Subzero Superfood Goji Berry 8oz.
Quantity: 400 pods (total)
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.
Delivered between May and June 2016
Where it was sold
FDA's distribution note: The firm refused to provide a distribution list. According to the firm products were gifted through a kickstarter website in which people received the product as a result of donating money.
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
- FMIF Holdings, LLC dba Snow Monkey
- Initiated by
- Voluntary: Firm initiated
- Recall initiated
- Nov 21, 2016
- In FDA report of
- Dec 21, 2016
- Terminated
- Feb 9, 2017
- FDA recall number
- F-0721-2017 · event 75771
- 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.