State
19,704 recalls have nationwide distribution and so reach California. 0 additional recalls listed California 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 California 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.
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.
Pending LLM rewrite. Source: FDA_FOOD H-0804-2026.
Pending LLM rewrite. Source: FDA_FOOD H-0801-2026.
Pending LLM rewrite. Source: FDA_FOOD H-0798-2026.
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-0816-2026.
Pending LLM rewrite. Source: FDA_FOOD H-0836-2026.
Pending LLM rewrite. Source: FDA_FOOD H-0819-2026.
Pending LLM rewrite. Source: FDA_FOOD H-0796-2026.
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.
Medtronic is recalling certain lots of its DLP Retrograde Cannula (Model 94915), a cardiopulmonary bypass vascular catheter, due to potential sterile barrier breach.
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-0808-2026.
Pending LLM rewrite. Source: FDA_FOOD H-0802-2026.
Pending LLM rewrite. Source: FDA_FOOD H-0833-2026.
Pending LLM rewrite. Source: FDA_FOOD H-0806-2026.
Pending LLM rewrite. Source: FDA_FOOD H-0835-2026.
Medtronic Perfusion Systems is recalling certain lots of the DLP Retrograde Cannula Model 94665 due to potential sterile barrier breach. The product is used in cardiopulmonary bypass procedures worldwide.
Pending LLM rewrite. Source: FDA_FOOD H-0795-2026.
Pending LLM rewrite. Source: FDA_FOOD H-0817-2026.
Pending LLM rewrite. Source: FDA_FOOD H-0818-2026.
Pending LLM rewrite. Source: FDA_FOOD H-0800-2026.
Pending LLM rewrite. Source: FDA_FOOD H-0814-2026.
Pending LLM rewrite. Source: FDA_FOOD H-0805-2026.
Pending LLM rewrite. Source: FDA_FOOD H-0803-2026.