State
19,713 recalls have nationwide distribution and so reach Minnesota. 0 additional recalls listed Minnesota 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 Minnesota 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: FDA_DEVICE Z-1128-2026.
Pending LLM rewrite. Source: FDA_DEVICE Z-1143-2026.
Pending LLM rewrite. Source: FDA_DEVICE Z-1132-2026.
Pending LLM rewrite. Source: FDA_DRUG D-0295-2026.
Pending LLM rewrite. Source: FDA_DEVICE Z-1149-2026.
Pending LLM rewrite. Source: FDA_DEVICE Z-1142-2026.
Pending LLM rewrite. Source: CPSC 26205.
Pending LLM rewrite. Source: CPSC 26215.
Pending LLM rewrite. Source: CPSC 26203.
Pending LLM rewrite. Source: CPSC 26210.
Pending LLM rewrite. Source: CPSC 26209.
Pending LLM rewrite. Source: CPSC 26208.
Pending LLM rewrite. Source: CPSC 26207.
Pending LLM rewrite. Source: CPSC 26201.
Pending LLM rewrite. Source: CPSC 26206.
Pending LLM rewrite. Source: CPSC 26202.
Pending LLM rewrite. Source: CPSC 26204.
Pending LLM rewrite. Source: FDA_DRUG D-0278-2026.
Pending LLM rewrite. Source: FDA_DEVICE Z-1061-2026.
Pending LLM rewrite. Source: FDA_DRUG D-0277-2026.
Pending LLM rewrite. Source: FDA_DEVICE Z-1040-2026.
Pending LLM rewrite. Source: FDA_DRUG D-0256-2026.
Pending LLM rewrite. Source: FDA_DEVICE Z-1070-2026.
Pending LLM rewrite. Source: FDA_DEVICE Z-1054-2026.
Pending LLM rewrite. Source: FDA_DEVICE Z-1090-2026.