Black Forge Knives 1- Name: Carbon Steel Utility Kitchen Knife Model: CSK1700 recall — FDA F-1641-2024

Recall record at a glance

Official product description

1- Name: Carbon Steel Utility Kitchen Knife Model: CSK1700 Size: Total length: 10.25" Type of packaging: Each knife packed in a single box 2- Name: Carbon Steel Utility Kitchen Cleaver Knife Model: CSK1701 Size: Total length: 10.5" Type of packaging: Each knife packed in a single box 3- Name: Carbon Steel Utility Kitchen Knife Model: 501141 Size: Total length: 9.5" Type of packaging: Each knife packed in a single box 4- Name: Burnt Bone & Carbon Steel Ulu Knife Model: 2432 Size: Total length: 4" Type of packaging: Each knife packed in a single box 5- Name: Rosewood Carbon Steel Ulu Knife Model: 501204 Size: Total length: 4" Type of packaging: Each knife packed in a single box 6- Name: Rosewood Carbon Steel Meat Cleaver Model: 501172 Size: Total length: 10.25" Type of packaging: Each knife packed in a single box Knives sold direct to consumers via Bespoke Post.

Why the product was recalled

Products contain elevated levels of lead.

Distribution information

GA and further distributed directly to consumers

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: E-Mail.

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.