State
19,702 recalls have nationwide distribution and so reach Arizona. 0 additional recalls listed Arizona 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 Arizona 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_FOOD H-0799-2026.
Becton, Dickinson and Company is recalling Swan-Ganz Jr Catheters (models SGPT54, SGPT64P, SGPT755P) because the blue proximal injectate lumen hub may leak or break due to manufacturing changes, risking infection, medication loss, and blood loss.
Pending LLM rewrite. Source: FDA_FOOD H-0831-2026.
Pending LLM rewrite. Source: FDA_FOOD H-0836-2026.
Pending LLM rewrite. Source: FDA_FOOD H-0833-2026.
Pending LLM rewrite. Source: FDA_FOOD H-0832-2026.
Pending LLM rewrite. Source: FDA_FOOD H-0796-2026.
Pending LLM rewrite. Source: FDA_FOOD H-0816-2026.
Pending LLM rewrite. Source: FDA_FOOD H-0835-2026.
Pending LLM rewrite. Source: FDA_FOOD H-0803-2026.
Medtronic Perfusion Systems is recalling certain lots of the DLP Retrograde Cannula (Model 94913), a cardiopulmonary bypass vascular catheter, due to a potential sterile barrier breach.
Pending LLM rewrite. Source: FDA_FOOD H-0801-2026.
Medtronic is recalling certain lots of DLP Retrograde Cannula (Model 94913L), a cardiopulmonary bypass catheter, due to potential sterile barrier breaches. The affected device was distributed worldwide.
Pending LLM rewrite. Source: FDA_FOOD H-0806-2026.
Pending LLM rewrite. Source: FDA_FOOD H-0797-2026.
Pending LLM rewrite. Source: FDA_FOOD H-0815-2026.
ICU Medical is recalling Oncology Kits with extension sets due to potential leaks that could interrupt chemotherapy infusion and expose hazardous substances to patients, caregivers, and pharmacy technicians.
Pending LLM rewrite. Source: FDA_FOOD H-0808-2026.
Philips Azurion X-ray imaging systems may experience impaired table movement due to mechanical wear in the Float Tabletop control. The control module defect could affect longitudinal and transverse table positioning during medical procedures.
Pending LLM rewrite. Source: FDA_FOOD H-0800-2026.
Becton, Dickinson and Company is recalling Swan-Ganz Pacing Catheter Model D200F7 due to a manufacturing defect that may cause the proximal injectate lumen hub to leak or break, potentially leading to infection, medication loss, or blood loss.
The deaeration hose in Philips Azurion X-ray tube cooling units may degrade over time and leak oil, affecting cooling performance and automatically triggering low-dose fluoroscopy mode.
Pending LLM rewrite. Source: FDA_FOOD H-0814-2026.
Pending LLM rewrite. Source: FDA_FOOD H-0804-2026.
Pending LLM rewrite. Source: FDA_FOOD H-0805-2026.