[pending] Minka Lighting Recalls Vortic Flow Series Lights Due to Impact Injury Hazard
Pending LLM rewrite. Source: CPSC 25301.
- Product
- Minka Vortic Flow Series light fixtures
- Category
- Consumer Product
- Distribution
- Distributed nationwide
State
19,789 recalls have nationwide distribution and so reach South Carolina. 0 additional recalls listed South Carolina 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 South Carolina 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 25301.
Pending LLM rewrite. Source: CPSC 25302.
Pending LLM rewrite. Source: CPSC 25305.
Pending LLM rewrite. Source: CPSC 25304.
Pending LLM rewrite. Source: CPSC 25307.
Pending LLM rewrite. Source: FDA_DEVICE Z-1789-2025.
Pending LLM rewrite. Source: FDA_DEVICE Z-1797-2025.
Pending LLM rewrite. Source: FDA_DRUG D-0441-2025.
Pending LLM rewrite. Source: FDA_DEVICE Z-1785-2025.
Pending LLM rewrite. Source: FDA_DEVICE Z-1794-2025.
Pending LLM rewrite. Source: FDA_DEVICE Z-1808-2025.
Pending LLM rewrite. Source: FDA_DEVICE Z-1799-2025.
Pending LLM rewrite. Source: FDA_DEVICE Z-1792-2025.
Pending LLM rewrite. Source: FDA_DEVICE Z-1806-2025.
Pending LLM rewrite. Source: FDA_DEVICE Z-1802-2025.
Pending LLM rewrite. Source: FDA_DEVICE Z-1787-2025.
Pending LLM rewrite. Source: FDA_DEVICE Z-1800-2025.
Pending LLM rewrite. Source: FDA_DEVICE Z-1796-2025.
Pending LLM rewrite. Source: FDA_DEVICE Z-1801-2025.
Pending LLM rewrite. Source: FDA_DEVICE Z-1803-2025.
Pending LLM rewrite. Source: FDA_DEVICE Z-1788-2025.
Pending LLM rewrite. Source: FDA_DEVICE Z-1807-2025.
Pending LLM rewrite. Source: FDA_DEVICE Z-1804-2025.
Pending LLM rewrite. Source: FDA_DEVICE Z-1790-2025.
Pending LLM rewrite. Source: FDA_DEVICE Z-1805-2025.