[pending] GEM Premier 5000 PAK; Part No. 00055360008.
Pending LLM rewrite. Source: FDA_DEVICE Z-1525-2026.
- Product
- GEM Premier 5000 PAK; Part No. 00055360008.
- Category
- Medical Device
- Distribution
- Distributed nationwide
State
19,704 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-1525-2026.
Pending LLM rewrite. Source: FDA_DEVICE Z-1496-2026.
Pending LLM rewrite. Source: FDA_DEVICE Z-1529-2026.
Pending LLM rewrite. Source: FDA_DEVICE Z-1500-2026.
Pending LLM rewrite. Source: FDA_DEVICE Z-1555-2026.
Pending LLM rewrite. Source: FDA_DEVICE Z-1556-2026.
Pending LLM rewrite. Source: FDA_DEVICE Z-1516-2026.
Pending LLM rewrite. Source: FDA_DEVICE Z-1502-2026.
Pending LLM rewrite. Source: FDA_DEVICE Z-1508-2026.
Pending LLM rewrite. Source: CPSC 26319.
Pending LLM rewrite. Source: CPSC 26323.
Pending LLM rewrite. Source: CPSC 26320.
Pending LLM rewrite. Source: CPSC 26324.
Pending LLM rewrite. Source: CPSC 26321.
Pending LLM rewrite. Source: FDA_DRUG D-0388-2026.
Pending LLM rewrite. Source: FDA_DEVICE Z-1490-2026.
Pending LLM rewrite. Source: FDA_DEVICE Z-1491-2026.
Pending LLM rewrite. Source: FDA_DRUG D-0356-2026.
Pending LLM rewrite. Source: FDA_DEVICE Z-1489-2026.
Pending LLM rewrite. Source: FDA_DRUG D-0385-2026.
Pending LLM rewrite. Source: FDA_DRUG D-0376-2026.
Pending LLM rewrite. Source: FDA_DRUG D-0367-2026.
Pending LLM rewrite. Source: NHTSA 24V900000.
Pending LLM rewrite. Source: FDA_DRUG D-0381-2026.
Pending LLM rewrite. Source: FDA_DEVICE Z-1482-2026.