FDA recall record

Starwest Botanicals Elderberry Whole Organic recall — FDA F-0115-2021

Direct customer tested product upon receipt and had a positive result for Salmonella.

Class Iclassification
F-0115-2021official record ID
Nov 18, 2020report date

Recall record at a glance

Official recordF-0115-2021
CategoryFood Recalls
ClassificationClass I
FDA record statusTerminated
Recalling firmStarwest Botanicals, Inc.
Report dateNov 18, 2020
Recall initiation dateOct 16, 2020
Quantity10,037 lbs. (total)
LocationSacramento, CA, United States

Official product description

Elderberry Whole Organic; Sambucus Nigra; Origin: Croatia Distributed in boxes with plastic liners. Various sizes Bulk UPC 7 67963 07314 3, Item # 209290-00 Starwest Botanicals,Inc. 161 Main Street, Sacramento, CA 95838 Certified Organic

Why the product was recalled

Direct customer tested product upon receipt and had a positive result for Salmonella.

Distribution information

Nationwide distribution Two Canadian Customers

How to read the classification

FDA Class I indicates a situation in which there is a reasonable probability that use of or exposure to the product will cause serious adverse health consequences or death. The classification shown here comes directly from the FDA enforcement record.

Additional record details

Recall type: Voluntary: Firm initiated. Initial notification: Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit.

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.

Related recall records

Other records from the same recalling company are shown first when available.