FDA recall record

Kroger Co Tender Twist 100% Whole Wheat Bread 24 oz recall — FDA F-1282-2013

The firm was notified of bread with traces of visible ink was discovered which later led to the discovery of plastic pen pieces.

Class IIclassification
F-1282-2013official record ID
Apr 10, 2013report date

Recall record at a glance

Official recordF-1282-2013
CategoryFood Recalls
ClassificationClass II
FDA record statusTerminated
Recalling firmKroger Co
Report dateApr 10, 2013
Recall initiation dateFeb 26, 2013
Quantity790/24 oz loaves
LocationCincinnati, OH, United States

Official product description

Tender Twist 100% Whole Wheat Bread 24 oz (1 LB 8 OZ) 680g***INGREDIENTS: UNBLEACHED ENRICHED FLOUR***CONTAINS: WHEAT, SOY. DISTRIBUTED BY THE KROGER CO. CINCINNATI, OHIO 45202" Sold under the following brand names: Fred Meyer & Goodyman

Why the product was recalled

The firm was notified of bread with traces of visible ink was discovered which later led to the discovery of plastic pen pieces.

Distribution information

Product was distributed to the following states: ID, OR & WA.

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: Press Release.

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.