Whole Foods Market Organic Muchi Curry Seasoning packaged in a glass bottle
Reason Product may be contaminated with Salmonella.
16 oz. foil packages of Frontier Co-op Hojicha Tea Certified Organic Camellia sinensus recall
Recalled by Frontier Natural Products CO-OP · Norway, IA, United States
Class II — Moderate risk. May cause temporary or reversible harm; serious harm unlikely.
Why it was recalled
Product potentially 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
16 oz. foil packages of Frontier Co-op Hojicha Tea Certified Organic Camellia sinensus, Norway, IA 52318
Quantity: Lot 4338:108-1 lb packages, lot 5096:69-1 lb packages, lot 5191:104-1 lb packages, lot 5289:139-1 lb packages, and lot 6042:25-1 lb packages
Food: Juice & beverages
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.
Item # 2920. Lot #s 4338 Best By Dec 2017, 5096 Best By Apr 2018, 5191 Best By Jul 2018, 5289 Best By Oct 2018, and 6042 Best By Feb 2019 UPC 089836029201
Where it was sold
Nationwide.
FDA's distribution note: Distribution included direct consumers and wholesale and distributors nationwide. A customer list was provided.
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
- Frontier Natural Products CO-OP
- Initiated by
- Voluntary: Firm initiated
- Recall initiated
- May 10, 2016
- In FDA report of
- Jun 15, 2016
- Terminated
- Oct 12, 2018
- FDA recall number
- F-1438-2016 · event 74119
- Official record
- FDA enforcement report search
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