Pumpkin Spice No Bake Cookie
Reason Peanuts & Eggs. The firm list peanuts in the ingredient statement but omitted them from the contain statement. They also have eggs listed in the contain statement but there are no eggs in the product.
Lee's Tea brand of Pink Chai recall
Recalled by Lee's Provisions INC · Toronto, N/A, Canada
Class II — Moderate risk. May cause temporary or reversible harm; serious harm unlikely.
Why it was recalled
Product may be 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
Lee's Tea brand of Pink Chai - Organic Spiced Tulsi Tea Blend Loose Leaf Tea packaged in re-sealable plastic pouches sizes 30g, UPC 6 28055 21014 6 and 90g, UPC 6 28055 21004 7.
Quantity: 6,788 units
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.
30g package: 3062718 06/2020; 90g Package: Lot #'s 2021JA23PC, 2021FE05PC, & 03-02021, Best Before 2021 MR21
Where it was sold
Nationwide.
Arizona New York
FDA's distribution note: Originated from Canadian exporter sold to 2 direct accounts in the US (Brooklyn, NY and Tempe, AZ). Both direct accounts further distributed the product in tact to customers throughout the U.S.
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
- Lee's Provisions INC
- Initiated by
- Voluntary: Firm initiated
- Recall initiated
- Mar 27, 2019
- In FDA report of
- May 15, 2019
- Terminated
- Oct 9, 2019
- FDA recall number
- F-1336-2019 · event 82711
- Official record
- FDA enforcement report search
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