[pending] 509 Recalls Helmets Due to Risk of Head Injury
Pending LLM rewrite. Source: CPSC 25374.
- Product
- 509 helmets and 509 for Polaris helmets
- Category
- Consumer Product
- Distribution
- Distributed nationwide
State
20,082 recalls have nationwide distribution and so reach New Jersey. 0 additional recalls listed New Jersey 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 New Jersey 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 25374.
Pending LLM rewrite. Source: NHTSA 23V236000.
Pending LLM rewrite. Source: CPSC 25369.
Pending LLM rewrite. Source: NHTSA 23V234000.
Pending LLM rewrite. Source: CPSC 25372.
Pending LLM rewrite. Source: NHTSA 23V233000.
Pending LLM rewrite. Source: NHTSA 25V149000.
Pending LLM rewrite. Source: CPSC 25366.
Pending LLM rewrite. Source: NHTSA 24V212000.
Pending LLM rewrite. Source: CPSC 25367.
Pending LLM rewrite. Source: CPSC 25371.
Pending LLM rewrite. Source: FDA_DRUG D-0494-2025.
Pending LLM rewrite. Source: FDA_DEVICE Z-2012-2025.
Pending LLM rewrite. Source: FDA_DEVICE Z-1997-2025.
Pending LLM rewrite. Source: FDA_DRUG D-0476-2025.
Pending LLM rewrite. Source: FDA_DRUG D-0487-2025.
Pending LLM rewrite. Source: NHTSA 25V061000.
Pending LLM rewrite. Source: FDA_DEVICE Z-2027-2025.
Pending LLM rewrite. Source: FDA_FOOD H-0092-2025.
Pending LLM rewrite. Source: FDA_DEVICE Z-2003-2025.
Pending LLM rewrite. Source: FDA_DEVICE Z-1995-2025.
Pending LLM rewrite. Source: FDA_DRUG D-0482-2025.
Pending LLM rewrite. Source: FDA_DRUG D-0490-2025.
Pending LLM rewrite. Source: FDA_DEVICE Z-2004-2025.
Pending LLM rewrite. Source: FDA_DEVICE Z-1904-2025.