[pending] Lutron Recalls Power Interfaces for LED Tape Lights Due to Shock Hazard
Pending LLM rewrite. Source: CPSC 25317.
- Product
- Lutron-branded power interfaces for LED tape lights
- Category
- Consumer Product
- Distribution
- Distributed nationwide
State
20,072 recalls have nationwide distribution and so reach West Virginia. 0 additional recalls listed West Virginia 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 West Virginia 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 25317.
Pending LLM rewrite. Source: CPSC 25314.
Pending LLM rewrite. Source: FDA_DEVICE Z-1822-2025.
Pending LLM rewrite. Source: FDA_DEVICE Z-1847-2025.
Pending LLM rewrite. Source: FDA_DEVICE Z-1850-2025.
Pending LLM rewrite. Source: FDA_DEVICE Z-1858-2025.
Pending LLM rewrite. Source: FDA_DEVICE Z-1864-2025.
Pending LLM rewrite. Source: FDA_DEVICE Z-1825-2025.
Pending LLM rewrite. Source: FDA_DEVICE Z-1875-2025.
Pending LLM rewrite. Source: FDA_DEVICE Z-1827-2025.
Pending LLM rewrite. Source: FDA_DEVICE Z-1824-2025.
Pending LLM rewrite. Source: FDA_DRUG D-0452-2025.
Pending LLM rewrite. Source: FDA_DEVICE Z-1821-2025.
Pending LLM rewrite. Source: FDA_DEVICE Z-1857-2025.
Pending LLM rewrite. Source: FDA_DEVICE Z-1876-2025.
Pending LLM rewrite. Source: FDA_DEVICE Z-1840-2025.
Pending LLM rewrite. Source: FDA_DEVICE Z-1861-2025.
Pending LLM rewrite. Source: FDA_DEVICE Z-1874-2025.
Pending LLM rewrite. Source: FDA_DEVICE Z-1831-2025.
Pending LLM rewrite. Source: FDA_DEVICE Z-1872-2025.
Pending LLM rewrite. Source: FDA_DEVICE Z-1856-2025.
Pending LLM rewrite. Source: FDA_DEVICE Z-1873-2025.
Pending LLM rewrite. Source: FDA_DEVICE Z-1851-2025.
Pending LLM rewrite. Source: FDA_DEVICE Z-1826-2025.
Pending LLM rewrite. Source: FDA_DEVICE Z-1843-2025.