[pending] Atlan A350. Model Number: 8211500. anesthesia workstation
Pending LLM rewrite. Source: FDA_DEVICE Z-2207-2026.
- Product
- Atlan A350. Model Number: 8211500. anesthesia workstation
- Category
- Medical Device
- Distribution
- 11 states
State
19,701 recalls have nationwide distribution and so reach Arkansas. 989 additional recalls listed Arkansas 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 Arkansas 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-2207-2026.
Pending LLM rewrite. Source: FDA_DEVICE Z-2307-2026.
Pending LLM rewrite. Source: FDA_DEVICE Z-2286-2026.
Pending LLM rewrite. Source: FDA_DEVICE Z-2262-2026.
Pending LLM rewrite. Source: FDA_FOOD H-0905-2026.
Pending LLM rewrite. Source: FDA_DRUG D-0565-2026.
Pending LLM rewrite. Source: FDA_FOOD H-0910-2026.
Pending LLM rewrite. Source: FDA_DRUG D-0566-2026.
Pending LLM rewrite. Source: FDA_DRUG D-0558-2026.
Pending LLM rewrite. Source: FDA_DRUG D-0554-2026.
Pending LLM rewrite. Source: FDA_DRUG D-0571-2026.
Pending LLM rewrite. Source: FDA_DRUG D-0552-2026.
Pending LLM rewrite. Source: FDA_DRUG D-0575-2026.
Pending LLM rewrite. Source: FDA_DRUG D-0562-2026.
Pending LLM rewrite. Source: FDA_DRUG D-0555-2026.
Pending LLM rewrite. Source: FDA_DRUG D-0569-2026.
Pending LLM rewrite. Source: FDA_DRUG D-0560-2026.
Pending LLM rewrite. Source: FDA_DEVICE Z-2257-2026.
Pending LLM rewrite. Source: FDA_DRUG D-0557-2026.
Pending LLM rewrite. Source: FDA_DEVICE Z-2285-2026.
Pending LLM rewrite. Source: FDA_DEVICE Z-2282-2026.
Pending LLM rewrite. Source: FDA_DEVICE Z-2273-2026.
Pending LLM rewrite. Source: FDA_DEVICE Z-2264-2026.
Pending LLM rewrite. Source: FDA_DEVICE Z-2250-2026.
Pending LLM rewrite. Source: FDA_DEVICE Z-2212-2026.