State
19,713 recalls have nationwide distribution and so reach Kansas. 0 additional recalls listed Kansas specifically in their distribution scope.
Most US product recalls have nationwide distribution — the manufacturer ships into every state and the recall sweeps the same way. We include those in this listing because they affect Kansas consumers even though the source notice doesn’t name the state. State-specific recalls are usually for products with regional distribution (a regional dairy, a local store brand) or where the agency was able to narrow the affected shipments to specific destinations.
If you’re checking whether a recall affects your purchase, the recall detail page lists the exact production lot codes, UPCs, and best-by dates. Match those against your package — distribution scope is a starting filter, not the final answer.
Pending LLM rewrite. Source: CPSC 26368.
Pending LLM rewrite. Source: CPSC 26381.
Pending LLM rewrite. Source: CPSC 26365.
Pending LLM rewrite. Source: CPSC 26379.
Pending LLM rewrite. Source: NHTSA 24V157000.
Pending LLM rewrite. Source: CPSC 26380.
Pending LLM rewrite. Source: CPSC 26373.
Pending LLM rewrite. Source: NHTSA 26V066000.
Pending LLM rewrite. Source: FDA_DEVICE Z-1599-2026.
Pending LLM rewrite. Source: FDA_DEVICE Z-1608-2026.
Pending LLM rewrite. Source: FDA_DEVICE Z-1577-2026.
Pending LLM rewrite. Source: NHTSA 25V012000.
Pending LLM rewrite. Source: FDA_DEVICE Z-1626-2026.
Western Mixers Produce & Nuts, Inc. is recalling Treasured Harvest brand Chilli Spanish Peanuts (25lb bags, Lot #260230) due to glass fragments found in sealed containers.
Pending LLM rewrite. Source: NHTSA 25V016000.
Pending LLM rewrite. Source: FDA_DEVICE Z-1566-2026.
Pending LLM rewrite. Source: FDA_DEVICE Z-1630-2026.
Pending LLM rewrite. Source: FDA_DRUG D-0403-2026.
Pending LLM rewrite. Source: NHTSA 25V015000.
Pending LLM rewrite. Source: FDA_DRUG D-0404-2026.
Pending LLM rewrite. Source: FDA_DEVICE Z-1634-2026.
Pending LLM rewrite. Source: FDA_DEVICE Z-1575-2026.
Pending LLM rewrite. Source: FDA_DEVICE Z-1606-2026.
Pending LLM rewrite. Source: FDA_DEVICE Z-1638-2026.
Pending LLM rewrite. Source: FDA_DRUG D-0401-2026.