FDA recall record

Walker Honey Co Blackberry Creamed Honey 671333101308 * These product labels recall — FDA H-0703-2026

Creamed honey products may contain stainless steel dust/flakes and/or small particles or shreds of plastic.

Class IIclassification
H-0703-2026official record ID
May 13, 2026report date

Recall record at a glance

Official recordH-0703-2026
CategoryFood Recalls
ClassificationClass II
FDA record statusOngoing
Recalling firmWalker Honey Co
Report dateMay 13, 2026
Recall initiation dateApr 3, 2026
Quantity2,650 units (Total)
LocationRogers, TX, United States

Official product description

Blackberry Creamed Honey 671333101308 * These product labels may also say Whipped Honey instead of Creamed Honey as labels and size were changed in this timeline from 14 oz Creamed Honey to 11 oz Whipped Honey.The UPC codes remained the same. Packaged in Glass jars UPC Code: 671333101308

Why the product was recalled

Creamed honey products may contain stainless steel dust/flakes and/or small particles or shreds of plastic.

Distribution information

Texas

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: 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.

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