State
19,702 recalls have nationwide distribution and so reach Maryland. 0 additional recalls listed Maryland 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 Maryland 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-0831-2026.
Pending LLM rewrite. Source: FDA_FOOD H-0832-2026.
Pending LLM rewrite. Source: FDA_FOOD H-0801-2026.
Pending LLM rewrite. Source: FDA_FOOD H-0797-2026.
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.
Philips is recalling Integris-Allura X-ray systems because deaeration hoses in X-ray tube cooling units may degrade, causing oil leakage that reduces cooling performance and triggers a system shutdown to low-dose mode.
Pending LLM rewrite. Source: FDA_FOOD H-0802-2026.
Medtronic is recalling certain lots of GUNDRY Retrograde Cannula (Model 94113T), a cardiopulmonary bypass catheter, due to potential sterile barrier breach in the product.
Pending LLM rewrite. Source: FDA_FOOD H-0804-2026.
Medtronic is recalling certain lots of its DLP Retrograde Cannula (Model 94915), a cardiopulmonary bypass vascular catheter, due to potential sterile barrier breach.
Pending LLM rewrite. Source: FDA_FOOD H-0817-2026.
Pending LLM rewrite. Source: FDA_FOOD H-0799-2026.
Pending LLM rewrite. Source: FDA_FOOD H-0808-2026.
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-0796-2026.
Pending LLM rewrite. Source: FDA_FOOD H-0835-2026.
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.
Pending LLM rewrite. Source: FDA_FOOD H-0814-2026.
Pending LLM rewrite. Source: FDA_FOOD H-0819-2026.
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-0833-2026.
Pending LLM rewrite. Source: FDA_FOOD H-0816-2026.
Pending LLM rewrite. Source: FDA_FOOD H-0836-2026.
Medtronic is recalling certain lots of GUNDRY Retrograde Cannula (Model 94115T) cardiopulmonary bypass vascular catheters due to potential sterile barrier breach. The affected product has been distributed worldwide.
Pending LLM rewrite. Source: FDA_FOOD H-0834-2026.