[pending] 2025 HEARTLAND CYCLONE
Pending LLM rewrite. Source: NHTSA 25V304000.
- Product
- HEARTLAND — 2025 HEARTLAND CYCLONE
- Category
- Vehicle
- Distribution
- Distributed nationwide
State
19,787 recalls have nationwide distribution and so reach Idaho. 0 additional recalls listed Idaho 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 Idaho 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: NHTSA 25V304000.
Pending LLM rewrite. Source: NHTSA 25V316000.
Pending LLM rewrite. Source: CPSC 25456.
Pending LLM rewrite. Source: NHTSA 25V225000.
Pending LLM rewrite. Source: NHTSA 25V218000.
Pending LLM rewrite. Source: NHTSA 25V226000.
Pending LLM rewrite. Source: CPSC 25458.
Pending LLM rewrite. Source: CPSC 25455.
Pending LLM rewrite. Source: NHTSA 25V216000.
Pending LLM rewrite. Source: FDA_DEVICE Z-2424-2025.
Pending LLM rewrite. Source: FDA_DEVICE Z-2419-2025.
Pending LLM rewrite. Source: FDA_DEVICE Z-2463-2025.
Pending LLM rewrite. Source: FDA_DEVICE Z-2410-2025.
Pending LLM rewrite. Source: FDA_DEVICE Z-2473-2025.
Pending LLM rewrite. Source: FDA_DEVICE Z-2418-2025.
Pending LLM rewrite. Source: FDA_DEVICE Z-2414-2025.
Pending LLM rewrite. Source: FDA_DRUG D-0598-2025.
Pending LLM rewrite. Source: FDA_DEVICE Z-2364-2025.
Pending LLM rewrite. Source: FDA_DEVICE Z-2380-2025.
Pending LLM rewrite. Source: FDA_DEVICE Z-2398-2025.
Pending LLM rewrite. Source: FDA_DEVICE Z-2443-2025.
Pending LLM rewrite. Source: FDA_DEVICE Z-2379-2025.
Pending LLM rewrite. Source: FDA_DEVICE Z-2362-2025.
Pending LLM rewrite. Source: FDA_DEVICE Z-2350-2025.
Pending LLM rewrite. Source: FDA_DEVICE Z-2342-2025.