[pending] 2024 KENWORTH T280
Pending LLM rewrite. Source: NHTSA 23V661000.
- Product
- KENWORTH — 2024 KENWORTH T280
- Category
- Vehicle
- Distribution
- Distributed nationwide
State
20,072 recalls have nationwide distribution and so reach Oklahoma. 0 additional recalls listed Oklahoma 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 Oklahoma 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 23V661000.
Pending LLM rewrite. Source: NHTSA 25V583000.
Pending LLM rewrite. Source: NHTSA 25V582000.
Pending LLM rewrite. Source: NHTSA 23V663000.
Pending LLM rewrite. Source: NHTSA 23V658000.
Pending LLM rewrite. Source: CPSC 25253.
Pending LLM rewrite. Source: CPSC 25251.
Pending LLM rewrite. Source: NHTSA 25V501000.
Pending LLM rewrite. Source: CPSC 25255.
Pending LLM rewrite. Source: CPSC 25250.
Pending LLM rewrite. Source: CPSC 25257.
Pending LLM rewrite. Source: CPSC 25252.
Pending LLM rewrite. Source: CPSC 25256.
Pending LLM rewrite. Source: CPSC 25254.
Pending LLM rewrite. Source: NHTSA 24V535000.
Pending LLM rewrite. Source: FDA_DEVICE Z-1638-2025.
Pending LLM rewrite. Source: FDA_DEVICE Z-1712-2025.
Pending LLM rewrite. Source: FDA_DEVICE Z-1687-2025.
Pending LLM rewrite. Source: FDA_DEVICE Z-1709-2025.
Pending LLM rewrite. Source: FDA_DEVICE Z-1685-2025.
Pending LLM rewrite. Source: FDA_DEVICE Z-1631-2025.
Pending LLM rewrite. Source: FDA_DEVICE Z-1637-2025.
Pending LLM rewrite. Source: FDA_DEVICE Z-1711-2025.
Pending LLM rewrite. Source: FDA_DEVICE Z-1634-2025.
Pending LLM rewrite. Source: FDA_DEVICE Z-1633-2025.