FDA recall record

Lee's Tea brand of Pink Chai - Organic Spiced Tulsi Tea Blend recall — FDA F-1336-2019

Product may be contaminated with Salmonella.

Class IIclassification
F-1336-2019official record ID
May 15, 2019report date

Recall record at a glance

Official recordF-1336-2019
CategoryFood Recalls
ClassificationClass II
FDA record statusTerminated
Recalling firmLEE'S PROVISIONS Inc.
Report dateMay 15, 2019
Recall initiation dateMar 27, 2019
Quantity6,788 units
LocationToronto, N/A, Canada

Official product description

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.

Why the product was recalled

Product may be contaminated with Salmonella.

Distribution information

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.

How to read the classification

FDA Class II indicates a situation in which use of or exposure to the product may cause temporary or medically reversible adverse health consequences, or where the probability of serious consequences is remote. The classification shown here comes from the FDA record.

Additional record details

Recall type: Voluntary: Firm initiated. Initial notification: E-Mail.

What to do next

If you believe you have the recalled product, use the recall number and firm information above to confirm the official notice and follow the instructions issued by the FDA, recalling firm, retailer or product manufacturer. For drugs and medical devices, decisions about treatment or medical care should be discussed with a qualified health professional.

About this record

Recall Lookup USA preserves the most complete source information successfully retrieved. We do not create missing facts or infer affected lots or VINs. The official record may still change, so use the identifier above when verifying current instructions.

FDA source limitation: openFDA enforcement reports are a reference dataset, not a live public-alert or recall-lifecycle service. FDA notes that enforcement-report status may not be updated after classification. Confirm current actions with the FDA, recalling firm or appropriate healthcare professional when relevant.