FDA recall record

Flora 16/1.24 oz recall — FDA F-1110-2014

Flora Double Ginger Herbal Tea Blend 1.24 oz was recalled due to contamination with Salmonella.

Class IIclassification
F-1110-2014official record ID
Dec 25, 2013report date

Recall record at a glance

Official recordF-1110-2014
CategoryFood Recalls
ClassificationClass II
FDA record statusTerminated
Recalling firmFlora Inc.
Report dateDec 25, 2013
Recall initiation dateNov 18, 2013
Quantity6024 boxes (16 tea bags per box)
LocationLynden, WA, United States

Official product description

Flora Double Ginger Herbal Tea Blend, 16/1.24 oz (35.2g) tea bags per package. UPC 0 61998 63757 9 The product is labeled in parts: "***DOUBLE GINGER HERBAL TEA BLEND***FLORA***CERTIFIED ORGANIC***FRESH-SEALED TEA BAGS***16***NET WT 1.24 oz***(35.2 g)***INGREDIENTS: GINGER ROOT, LEMONGRASS HERB, PEPPERMINT LEAVES, LICORICE ROOT, BLACK PEPPER SEEDS, *ORGANIC***IMPORTED BY: FLORA INC., 805 E. BADGER RD. LYNDEN, WA***".

Why the product was recalled

Flora Double Ginger Herbal Tea Blend 1.24 oz was recalled due to contamination with Salmonella.

Distribution information

Distributed in the following states: FL, GA, IL, IN, KY, MD, MI, NC, NJ, NV, NY, OH, PA, and SC.

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: Letter.

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.