FDA recall record

Royal Rye KrustaVita Bread of Life brand Sourdough Dark Rye Bread recall — FDA F-1984-2014

Royal Rye LLC is recalling their KrustaVita Bread of Life rye bread due to undeclared soy.

Class IIclassification
F-1984-2014official record ID
Jun 11, 2014report date

Recall record at a glance

Official recordF-1984-2014
CategoryFood Recalls
ClassificationClass II
FDA record statusTerminated
Recalling firmRoyal Rye LLC
Report dateJun 11, 2014
Recall initiation dateMay 20, 2014
Quantity128 loaves
LocationHillsboro, OR, United States

Official product description

KrustaVita Bread of Life brand Sourdough Dark Rye Bread; Net Weight 20 oz (1.25 lb); packed in a clear plastic bag. UPC: 8 5243000200 6.

Why the product was recalled

Royal Rye LLC is recalling their KrustaVita Bread of Life rye bread due to undeclared soy.

Distribution information

Bread was distributed to 16 retail makets in Oregon and 1 retail market in Washington.

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: Telephone.

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.