[pending] 2024 GRAND DESIGN MOMENTUM
Pending LLM rewrite. Source: NHTSA 25V281000.
- Product
- GRAND DESIGN — 2024 GRAND DESIGN MOMENTUM
- Category
- Vehicle
- Distribution
- Distributed nationwide
State
19,789 recalls have nationwide distribution and so reach Arkansas. 0 additional recalls listed Arkansas 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 Arkansas 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 25V281000.
Pending LLM rewrite. Source: CPSC 25326.
Pending LLM rewrite. Source: CPSC 25315.
Pending LLM rewrite. Source: CPSC 25311.
Pending LLM rewrite. Source: NHTSA 25V291000.
Pending LLM rewrite. Source: CPSC 25317.
Pending LLM rewrite. Source: NHTSA 23V384000.
Pending LLM rewrite. Source: CPSC 25319.
Pending LLM rewrite. Source: CPSC 25313.
Pending LLM rewrite. Source: CPSC 25318.
Pending LLM rewrite. Source: CPSC 25323.
Pending LLM rewrite. Source: CPSC 25320.
Pending LLM rewrite. Source: CPSC 25325.
Pending LLM rewrite. Source: CPSC 25316.
Pending LLM rewrite. Source: CPSC 25322.
Pending LLM rewrite. Source: CPSC 25324.
Pending LLM rewrite. Source: CPSC 25321.
Pending LLM rewrite. Source: CPSC 25312.
Pending LLM rewrite. Source: CPSC 25314.
Pending LLM rewrite. Source: FDA_DEVICE Z-1822-2025.
Pending LLM rewrite. Source: FDA_DEVICE Z-1858-2025.
Pending LLM rewrite. Source: FDA_DRUG D-0448-2025.
Pending LLM rewrite. Source: FDA_DEVICE Z-1832-2025.
Pending LLM rewrite. Source: FDA_DRUG D-0450-2025.
Pending LLM rewrite. Source: FDA_DEVICE Z-1836-2025.