Traditional Medicinals Throat Coat Lemon Echinacea
Reason Vendor has determined that portions of a large raw material lot were positive for Salmonella.
Traditional Medinicals organic EveryDay Detox Lemon recall
Recalled by Traditional Medicinals Inc · Sebastopol, CA, United States
Class II — Moderate risk. May cause temporary or reversible harm; serious harm unlikely.
Why it was recalled
Vendor has determined that portions of a large raw material lot were positive for 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
Traditional Medinicals organic EveryDay Detox Lemon; Naturally Caffeine Free Herbal Tea; 16 wrapped tea bags - Herbal Supplement NET WT .85 oz (24g) UPC: 32917-00197
Quantity: 9108 cases (6 cartons per case, 16 teabags per carton)
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 Number:19461 ; Expiration Date: January 2021
Where it was sold
FDA's distribution note: US distribution and on distributor in Mexico
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
- Traditional Medicinals Inc
- Initiated by
- Voluntary: Firm initiated
- Recall initiated
- Apr 16, 2018
- In FDA report of
- May 2, 2018
- Terminated
- Jun 1, 2018
- FDA recall number
- F-1143-2018 · event 79856
- 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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