State
20,364 recalls have nationwide distribution and so reach Oklahoma. 0 additional recalls listed Oklahoma 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 Oklahoma 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.
American Woodmark Corporation is recalling about 235,000 Continental Cabinets and Hampton Bay kitchen wall cabinets that can detach from walls, posing an impact hazard. The company will provide free repair kits with brackets and installation assistance.
DYNAMITE SUPER capsule is being recalled nationwide because it was marketed without FDA approval and contains undeclared sildenafil and tadalafil, active ingredients used in sexual enhancement products.
The FDA recalls NUX Male Enhancement capsules distributed nationwide because they contain undeclared sildenafil and tadalafil, making them an unapproved drug. Consumers should not use this product.
Pro Power Knight Plus capsules contain undeclared sildenafil and tadalafil, prescription ingredients not listed on the label. The product was marketed as an unapproved drug and poses safety risks.
Cargill is recalling PROSANTE soy flour bearing a gluten-free claim because the products may contain gluten at levels above 20 ppm.
Family Dollar Stores is recalling Advil Liqui-Gels 200 mg ibuprofen capsules (SKUs 0999841 and 0916071) distributed nationwide due to storage outside labeled temperature requirements.
Inpeco laboratory automation systems have a firmware defect that may cause sample ID mis-association, leading to incorrect test results for electrolyte measurements. Potential consequences include abnormal treatment decisions and serious health complications.
Stryker Corporation is recalling SafeLight Fiber Optic Cables due to insufficient epoxy on the proximal end, which can cause light output failure and potentially delay surgical procedures.
Cargill is recalling PROSANTE TVGPTN products labeled as gluten-free because they may contain gluten levels above 20 ppm. The recall affects 42,400 pounds distributed nationwide and internationally.
A firmware bug in Inpeco laboratory automation modules may cause sample misidentification, leading to incorrect electrolyte test results and potential treatment errors.
Weleda Inc is recalling Hepatodoron® tablets due to potential metal contamination. The affected batch (J033, expiring January 31, 2027) was distributed nationwide.
Beaver Visitec is recalling the CryoTreQ Aa ophthalmic surgical instrument due to risk of sudden disassembly during use. Device disassembly during cryosurgery could cause permanent vision impairment.
Cargill is recalling Prosante TVGPTN food products labeled as gluten-free that may contain gluten above 20 ppm.
Cargill is recalling PROSANTE TVGPTN 3018B FLK poultry ingredient because products labeled gluten-free may contain gluten levels above 20 ppm, the legal threshold for gluten-free claims.
Steris surgical light handle covers may detach during use, risking contamination of the sterile field and patient injury. The FDA is recalling approximately 1.4 million affected covers.
Cargill is recalling PROSANTE soy flour products labeled gluten-free because they may contain gluten levels above 20 ppm, the FDA's regulatory threshold for gluten-free labeling. Products were distributed nationwide and internationally.
Cargill recalls 174,600 lbs of bulk ingredient distributed nationwide and internationally. Products labeled gluten-free contain gluten levels exceeding 20 ppm.
Cargill is recalling PROSANTE TSOYFLR soy flour labeled as gluten-free that may contain gluten exceeding safe limits (20 ppm). The product was distributed nationwide and internationally.
Tesla is recalling certain 2017-2021 Model 3, S, X, and Y vehicles due to a software error that may cause false forward-collision warnings or unexpected automatic emergency brake activation. No injuries have been reported.
Cargill is recalling approximately 110,650 pounds of PROSANTE TVGPTN 12B products labeled as gluten-free because they may contain gluten above the safe threshold.
PD-Rx Pharmaceuticals is voluntarily recalling 520 bottles of Simvastatin USP 20 mg nationwide due to manufacturing process quality control deviations. No adverse events have been reported.
ASO LLC is recalling Walgreens assorted bandages (item 196568) distributed nationwide due to benzalkonium chloride in the adhesive pad that is not disclosed on the labeling.
Cargill is recalling 36,000 lbs of grain products labeled as gluten-free that may contain gluten above the FDA safety limit. Consumers with celiac disease or gluten sensitivity should not consume affected product code 110026470-02523CHXEA.
Cargill recalls 977,000 pounds of soy flour products labeled gluten-free that may contain gluten above FDA limits. Products were distributed in the US and multiple countries.
Cargill is recalling PROSANTE soyflour products labeled gluten-free because they may contain gluten levels above 20 ppm, the FDA's threshold for gluten-free claims. People with celiac disease or gluten sensitivity should not consume these products.