ShanTea Ride The Dragon Honeybush/Licorice
Reason This recall has been initiated due to the potential for the possibility of Salmonella contamination.
ShanTea Enlightened Mind Mate/Kukicha recall
Recalled by ShanTea LLC · Mount Laurel, NJ, United States
Class II — Moderate risk. May cause temporary or reversible harm; serious harm unlikely.
Why it was recalled
This recall has been initiated due to the potential for the possibility of Salmonella contamination.
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
ShanTea Enlightened Mind Mate/Kukicha (UPC 794504284102) USDA Organic.
Quantity: 111 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 1354
Where it was sold
Arizona Florida Illinois Maryland New Jersey New York Ohio Oklahoma Pennsylvania Virginia Wisconsin
FDA's distribution note: Arizona, Califorina, Florida, Illinois, Maryland, New Jersey, New York, Ohio, Oklahoma, Pennsylvania, Virginia, Wisconsin,
Check the codes, then return or discard. Class II means eating it may cause temporary or reversible health problems. If your package matches the recalled codes, do not eat it - return it to the store or throw it away. 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
- ShanTea LLC
- Initiated by
- Voluntary: Firm initiated
- Recall initiated
- Mar 6, 2013
- In FDA report of
- Apr 17, 2013
- Terminated
- Mar 11, 2015
- FDA recall number
- F-1305-2013 · event 64801
- 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.