State
19,713 recalls have nationwide distribution and so reach Oregon. 0 additional recalls listed Oregon 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 Oregon 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 26256.
Pending LLM rewrite. Source: CPSC 26248.
Pending LLM rewrite. Source: CPSC 26249.
Pending LLM rewrite. Source: CPSC 26250.
Pending LLM rewrite. Source: CPSC 26251.
Pending LLM rewrite. Source: CPSC 26238.
Pending LLM rewrite. Source: CPSC 26246.
Pending LLM rewrite. Source: CPSC 26239.
Pending LLM rewrite. Source: CPSC 26240.
Pending LLM rewrite. Source: NHTSA 25V273000.
Pending LLM rewrite. Source: CPSC 26253.
Pending LLM rewrite. Source: NHTSA 25V245000.
Pending LLM rewrite. Source: FDA_DEVICE Z-1218-2026.
Pending LLM rewrite. Source: FDA_DEVICE Z-1220-2026.
Pending LLM rewrite. Source: FDA_DEVICE Z-1169-2026.
Pending LLM rewrite. Source: FDA_DEVICE Z-1166-2026.
Pending LLM rewrite. Source: FDA_DEVICE Z-1167-2026.
Pending LLM rewrite. Source: NHTSA 24V295000.
Pending LLM rewrite. Source: FDA_DEVICE Z-1170-2026.
Pending LLM rewrite. Source: FDA_DRUG D-0296-2026.
Pending LLM rewrite. Source: FDA_DEVICE Z-1215-2026.
Pending LLM rewrite. Source: FDA_DEVICE Z-1173-2026.
Pending LLM rewrite. Source: FDA_DRUG D-0300-2026.
Pending LLM rewrite. Source: FDA_DEVICE Z-1194-2026.
Pending LLM rewrite. Source: FDA_DEVICE Z-1186-2026.