[pending] Extended Tip Applicator, 8CM, Box of 5.
Pending LLM rewrite. Source: FDA_DEVICE Z-1958-2025.
- Product
- Extended Tip Applicator, 8CM, Box of 5.
- Category
- Medical Device
- Distribution
- Distributed nationwide
State
19,788 recalls have nationwide distribution and so reach Idaho. 0 additional recalls listed Idaho 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 Idaho 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-1958-2025.
Pending LLM rewrite. Source: FDA_FOOD H-0091-2025.
Pending LLM rewrite. Source: FDA_DEVICE Z-1996-2025.
Pending LLM rewrite. Source: FDA_DRUG D-0474-2025.
Pending LLM rewrite. Source: NHTSA 25V069000.
Pending LLM rewrite. Source: FDA_DEVICE Z-2028-2025.
Pending LLM rewrite. Source: FDA_DEVICE Z-2024-2025.
Pending LLM rewrite. Source: NHTSA 25V002000.
Pending LLM rewrite. Source: NHTSA 23V038000.
Pending LLM rewrite. Source: NHTSA 24V029000.
Pending LLM rewrite. Source: CPSC 25359.
Pending LLM rewrite. Source: CPSC 25360.
Pending LLM rewrite. Source: CPSC 25357.
Pending LLM rewrite. Source: CPSC 25361.
Pending LLM rewrite. Source: CPSC 25358.
Pending LLM rewrite. Source: CPSC 25354.
Pending LLM rewrite. Source: CPSC 25355.
Pending LLM rewrite. Source: CPSC 25353.
Pending LLM rewrite. Source: CPSC 25706.
Pending LLM rewrite. Source: CPSC 25362.
Pending LLM rewrite. Source: FDA_DEVICE Z-1976-2025.
Pending LLM rewrite. Source: FDA_DEVICE Z-1980-2025.
Pending LLM rewrite. Source: FDA_DEVICE Z-1978-2025.
Pending LLM rewrite. Source: FDA_DRUG D-0471-2025.
Pending LLM rewrite. Source: FDA_DEVICE Z-1982-2025.