[pending] nvyue Magic Pocket Staffs Recalled Due to Projectile and Laceration Hazards; Imported by Xingwenfeng
Pending LLM rewrite. Source: CPSC 26409.
- Product
- nvyue Magic Pocket Staffs
- Category
- Consumer Product
- Distribution
- Distributed nationwide
State
19,713 recalls have nationwide distribution and so reach Colorado. 0 additional recalls listed Colorado 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 Colorado 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 26409.
Pending LLM rewrite. Source: CPSC 26428.
Pending LLM rewrite. Source: CPSC 26420.
Pending LLM rewrite. Source: FDA_DEVICE Z-1723-2026.
Pending LLM rewrite. Source: FDA_DRUG D-0448-2026.
Pending LLM rewrite. Source: FDA_DEVICE Z-1727-2026.
Pending LLM rewrite. Source: FDA_DEVICE Z-1714-2026.
Pending LLM rewrite. Source: FDA_DRUG D-0434-2026.
Pending LLM rewrite. Source: FDA_DEVICE Z-1769-2026.
Pending LLM rewrite. Source: FDA_DRUG D-0439-2026.
Pending LLM rewrite. Source: FDA_DEVICE Z-1712-2026.
Pending LLM rewrite. Source: FDA_DRUG D-0441-2026.
Pending LLM rewrite. Source: FDA_DEVICE Z-1722-2026.
Pending LLM rewrite. Source: FDA_DEVICE Z-1725-2026.
Pending LLM rewrite. Source: FDA_DEVICE Z-1726-2026.
Pending LLM rewrite. Source: FDA_DEVICE Z-1721-2026.
Pending LLM rewrite. Source: FDA_DEVICE Z-1718-2026.
Pending LLM rewrite. Source: FDA_DRUG D-0428-2026.
Pending LLM rewrite. Source: FDA_DRUG D-0438-2026.
Pending LLM rewrite. Source: FDA_DEVICE Z-1730-2026.
Pending LLM rewrite. Source: FDA_DRUG D-0437-2026.
Pending LLM rewrite. Source: FDA_DEVICE Z-1729-2026.
Pending LLM rewrite. Source: FDA_DEVICE Z-1793-2026.
Pending LLM rewrite. Source: FDA_DRUG D-0431-2026.
Pending LLM rewrite. Source: FDA_DEVICE Z-1724-2026.