[pending] 2024 FOREST RIVER NO BOUNDARIES
Pending LLM rewrite. Source: NHTSA 24V137000.
- Product
- FOREST RIVER — 2024 FOREST RIVER NO BOUNDARIES
- Category
- Vehicle
- Distribution
- Distributed nationwide
State
19,713 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 24V137000.
Pending LLM rewrite. Source: NHTSA 24V139000.
Pending LLM rewrite. Source: NHTSA 24V037000.
Pending LLM rewrite. Source: NHTSA 24V036000.
Pending LLM rewrite. Source: CPSC 26060.
Pending LLM rewrite. Source: CPSC 26055.
Pending LLM rewrite. Source: CPSC 26052.
Pending LLM rewrite. Source: CPSC 26051.
Pending LLM rewrite. Source: CPSC 26063.
Pending LLM rewrite. Source: CPSC 26066.
Pending LLM rewrite. Source: CPSC 26065.
Pending LLM rewrite. Source: CPSC 26058.
Pending LLM rewrite. Source: CPSC 26061.
Pending LLM rewrite. Source: CPSC 26064.
Pending LLM rewrite. Source: CPSC 26059.
Pending LLM rewrite. Source: CPSC 26057.
Pending LLM rewrite. Source: CPSC 26053.
Pending LLM rewrite. Source: CPSC 26054.
Pending LLM rewrite. Source: CPSC 26062.
Pending LLM rewrite. Source: FDA_FOOD H-0149-2026.
Pending LLM rewrite. Source: FDA_DRUG D-0032-2026.
Pending LLM rewrite. Source: FDA_DRUG D-0036-2026.
Pending LLM rewrite. Source: FDA_DEVICE Z-0239-2026.
Pending LLM rewrite. Source: FDA_DRUG D-0096-2026.
Pending LLM rewrite. Source: FDA_DEVICE Z-0233-2026.