State
19,611 recalls have nationwide distribution and so reach New Hampshire. 0 additional recalls listed New Hampshire 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 New Hampshire 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.
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-0816-2026.
Pending LLM rewrite. Source: FDA_FOOD H-0798-2026.
Pending LLM rewrite. Source: FDA_FOOD H-0815-2026.
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-0801-2026.
Pending LLM rewrite. Source: FDA_FOOD H-0795-2026.
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-0831-2026.
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-0834-2026.
Pending LLM rewrite. Source: FDA_FOOD H-0803-2026.
Tangent Endoscopy is recalling its Tangent Single Use Digital Catheter (models TNG4002-IND and TNG-4007-6pk) due to fractures observed at the distal shaft tip without complete detachment, posing a risk during endoscopic procedures.
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-0805-2026.
Pending LLM rewrite. Source: FDA_FOOD H-0832-2026.
Pending LLM rewrite. Source: FDA_FOOD H-0819-2026.
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-0797-2026.
Pending LLM rewrite. Source: FDA_FOOD H-0806-2026.
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-0799-2026.
Pending LLM rewrite. Source: FDA_FOOD H-0836-2026.
Medtronic is recalling certain lots of GUNDRY Retrograde Cannula (Model 94113T), a cardiopulmonary bypass catheter, due to potential sterile barrier breach in the product.