Honeyville YELLOW COLOR
Reason Undeclared Red #40.
Herbal Tea Variety recall
Recalled by U S Deer Antlers Export & Import · Los Angeles, CA, United States
Class I — High risk. Reasonable probability of serious harm or death.
Why it was recalled
US Deer Antler Export and Import is recalling a variety of Herbal Teas because they may be contaminated with Clostridium botulinum
Pathogen: Botulism
Clostridium botulinum toxin, a risk in improperly canned or under-processed foods.
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
Herbal Tea Variety 120 ml/pouch, 40 pouches/case
Quantity: 9,480 units
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.
Herbal Tea Variety Batches prepared on premise between 3/1/17 and 4/30/17
Where it was sold
California Georgia Hawaii Illinois Maryland Missouri North Carolina New Jersey New York Oklahoma Pennsylvania Texas Virginia Washington
FDA's distribution note: US: CA, TX, NC, NY, VA, HI, GA, WA, IL, PA, OK, MO, MD, NJ. Korea.
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
- U S Deer Antlers Export & Import
- Initiated by
- Voluntary: Firm initiated
- Recall initiated
- May 2, 2017
- In FDA report of
- May 31, 2017
- Terminated
- Jun 14, 2017
- FDA recall number
- F-2249-2017 · event 77173
- Official record
- FDA enforcement report search
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