State
19,704 recalls have nationwide distribution and so reach South Dakota. 0 additional recalls listed South Dakota 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 South Dakota 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.
Giantex and Costway portable steam saunas are recalled because the steam diffuser can position too close to the user's body, causing burns. Giantex has received nine burn reports, including one second-degree burn.
Giantex outdoor lounge chairs model NP10025NY pose an amputation risk when adjusting the backrest due to exposed pinch points. One finger amputation has been reported.
Daoen Inc. is recalling Zen Fidget Magnetic Ball Sets because the loose high-powered magnets can be swallowed by children, causing intestinal perforation, blockage, or death. No injuries have been reported.
Tzumi Electronics is recalling SLF Sauna Blankets that can overheat, posing fire and burn hazards. Six reports of overheating have been received, including five with minor property damage.
Proudly American Store is recalling about 8,000 VL2020 lithium coin batteries sold on Amazon because they lack required child-resistant packaging and warning labels. Swallowed batteries can cause serious internal injuries and death.
Medtronic Perfusion Systems is recalling certain lots of the DLP Retrograde Cannula (Model 94215T) due to a potential sterile barrier breach. The affected product is a cardiopulmonary bypass vascular catheter distributed worldwide.
Zydus Pharmaceuticals is recalling Erythromycin Tablets, 250 mg, nationwide because certain lots contain N-Nitroso-Desmethyl-Erythromycin above the recommended acceptable intake limit due to CGMP deviations.
Medtronic is recalling certain lots of its DLP Retrograde Cannula (Model 94725), a cardiopulmonary bypass catheter, because the sterile barrier may be breached, potentially allowing contamination. The cannulas were distributed worldwide.
UCB Biosciences is recalling CIMZIA (certolizumab pegol) prefilled syringes nationwide because of a lack of assurance of sterility. Affected lots are distributed across the US.
Wisconsin Pharmacal Company is recalling MG217 Multi-Symptom Treatment Cream & Skin Protectant due to confirmed presence of Staphylococcus aureus contamination. Affected units are 6 oz tubes with Lot #1024088, expiring 11/30/2026, distributed nationwide and in the Bahamas.
Zydus Pharmaceuticals is recalling erythromycin 500 mg tablets nationwide due to the presence of N-Nitroso-Desmethyl-Erythromycin above the recommended acceptable intake limit, resulting from manufacturing deviations.
Becton, Dickinson and Company is recalling multiple models of Swan-Ganz Catheters due to potential leaking or breaking of the proximal injectate lumen hub that could lead to infection, medication loss, or 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.
Pending LLM rewrite. Source: FDA_FOOD H-0815-2026.
Pending LLM rewrite. Source: FDA_FOOD H-0805-2026.
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-0807-2026.
Pending LLM rewrite. Source: FDA_FOOD H-0814-2026.
Pending LLM rewrite. Source: FDA_FOOD H-0795-2026.
Pending LLM rewrite. Source: FDA_FOOD H-0835-2026.
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-0804-2026.
Pending LLM rewrite. Source: FDA_FOOD H-0801-2026.
Pending LLM rewrite. Source: FDA_FOOD H-0803-2026.
Pending LLM rewrite. Source: FDA_FOOD H-0800-2026.