[pending] Blood/EMB, Levine 100/PK, Product Number R02041
Pending LLM rewrite. Source: FDA_DEVICE Z-2225-2025.
- Product
- Blood/EMB, Levine 100/PK, Product Number R02041
- Category
- Medical Device
- Distribution
- Distributed nationwide
State
19,789 recalls have nationwide distribution and so reach Connecticut. 0 additional recalls listed Connecticut 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 Connecticut 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-2225-2025.
Pending LLM rewrite. Source: FDA_DEVICE Z-2172-2025.
Pending LLM rewrite. Source: FDA_DEVICE Z-2203-2025.
Pending LLM rewrite. Source: FDA_DEVICE Z-2223-2025.
Pending LLM rewrite. Source: FDA_DEVICE Z-2216-2025.
Pending LLM rewrite. Source: FDA_DEVICE Z-2177-2025.
Pending LLM rewrite. Source: FDA_DEVICE Z-2209-2025.
Pending LLM rewrite. Source: FDA_DEVICE Z-2230-2025.
Pending LLM rewrite. Source: NHTSA 24V461000.
Pending LLM rewrite. Source: FDA_DEVICE Z-2232-2025.
Pending LLM rewrite. Source: FDA_DRUG D-0543-2025.
Pending LLM rewrite. Source: NHTSA 24V460000.
Pending LLM rewrite. Source: FDA_FOOD H-0381-2025.
Pending LLM rewrite. Source: FDA_DEVICE Z-2214-2025.
Pending LLM rewrite. Source: FDA_DEVICE Z-2215-2025.
Pending LLM rewrite. Source: FDA_DRUG D-0547-2025.
Pending LLM rewrite. Source: NHTSA 24V459000.
Pending LLM rewrite. Source: FDA_DEVICE Z-2235-2025.
Pending LLM rewrite. Source: FDA_DEVICE Z-2161-2025.
Pending LLM rewrite. Source: FDA_DEVICE Z-2212-2025.
Pending LLM rewrite. Source: FDA_DEVICE Z-2221-2025.
Pending LLM rewrite. Source: NHTSA 25V298000.
Pending LLM rewrite. Source: NHTSA 25V302000.
Pending LLM rewrite. Source: NHTSA 25V282000.
Pending LLM rewrite. Source: NHTSA 25V297000.