[pending] SNOOZ Recalls Electrical Fans Due to Fire Hazard
Pending LLM rewrite. Source: CPSC 26388.
- Product
- Breez 2-in-1 Smart Bedroom Fan and White Noise Machine
- Category
- Consumer Product
- Distribution
- Distributed nationwide
State
19,704 recalls have nationwide distribution and so reach Pennsylvania. 0 additional recalls listed Pennsylvania 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 Pennsylvania 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 26388.
Pending LLM rewrite. Source: CPSC 26394.
Pending LLM rewrite. Source: CPSC 26392.
Pending LLM rewrite. Source: CPSC 26405.
Pending LLM rewrite. Source: CPSC 26386.
Pending LLM rewrite. Source: CPSC 26393.
Pending LLM rewrite. Source: CPSC 26398.
Pending LLM rewrite. Source: CPSC 26401.
Pending LLM rewrite. Source: CPSC 26385.
Pending LLM rewrite. Source: CPSC 26389.
Pending LLM rewrite. Source: CPSC 26395.
Pending LLM rewrite. Source: CPSC 26387.
Pending LLM rewrite. Source: FDA_DEVICE Z-1701-2026.
Pending LLM rewrite. Source: FDA_DEVICE Z-1763-2026.
Pending LLM rewrite. Source: FDA_DEVICE Z-1667-2026.
Pending LLM rewrite. Source: FDA_DEVICE Z-1759-2026.
Pending LLM rewrite. Source: FDA_DEVICE Z-1695-2026.
Pending LLM rewrite. Source: FDA_DEVICE Z-1743-2026.
Pending LLM rewrite. Source: FDA_DEVICE Z-1649-2026.
Pending LLM rewrite. Source: FDA_DEVICE Z-1675-2026.
Pending LLM rewrite. Source: FDA_DEVICE Z-1670-2026.
Pending LLM rewrite. Source: FDA_DEVICE Z-1664-2026.
Pending LLM rewrite. Source: FDA_DRUG D-0478-2026.
Pending LLM rewrite. Source: FDA_DRUG D-0408-2026.
Pending LLM rewrite. Source: FDA_DEVICE Z-1682-2026.