Food Recall Check
Class I · High risk Terminated Initiated Mar 6, 2018 (9 years ago)

Cardamom Pods Green Whole Organic Sold in recall

Recalled by Starwest Botanicals, Inc · Sacramento, CA, United States

Class I — High risk. Reasonable probability of serious harm or death.

Why it was recalled

Customer notified firm after they received a positive result for Salmonella of Lot #90186-00 Cardamon Pods Green Whole Organic supplied by Starwest Botanicals

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

Cardamom Pods Green Whole Organic Sold in 25 lb. bulk boxes and 1 lb. retail plastic bags UPC 1 pound bags: 7-6796302528-9; UPC bulk: 7 679630257-2 Imported from Guatemala Starwest Botanicals, Sacramento, CA

Quantity: 810 pounds of bulk and 133 x 1 lb. bags

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.

Bulk lot #90186-00, Item number 1 lb. bags lot 75593, Item number 209735-01

Where it was sold

FDA's distribution note: US and Canada

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
Starwest Botanicals, Inc
Initiated by
Voluntary: Firm initiated
Recall initiated
Mar 6, 2018
In FDA report of
Mar 21, 2018
Terminated
Jul 6, 2018
FDA recall number
F-0971-2018 · event 79465
Official record
FDA enforcement report search

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