State
20,364 recalls have nationwide distribution and so reach Florida. 0 additional recalls listed Florida 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 Florida 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.
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.
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.
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.
Philips is recalling certain ProxiDiagnost N90 radiography systems due to a cable under the table that may break. A broken cable could prevent users from tilting the table or engaging braking.
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 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 174,600 lbs of bulk ingredient distributed nationwide and internationally. Products labeled gluten-free contain gluten levels exceeding 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.
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's PROSANTE brand flour products labeled gluten-free may contain gluten above 20 ppm. The products were distributed nationwide across the US and internationally.
Cargill is recalling PROSANTE vegetable protein products labeled gluten-free due to potential gluten contamination exceeding 20 ppm. Consumers should check product codes and discard or return affected items.
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.
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.
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.
Jayco is recalling 2024 Precept and Entegra Coach Vision XL motorhomes because their window shades may obstruct emergency exit windows. Obstructed emergency exits could delay occupant evacuation during emergencies.
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.
Inpeco is recalling Alinity h laboratory automation system firmware that may mis-identify samples, causing incorrect electrolyte test results that could lead to improper patient treatment.
Cargill's Prosante products labeled gluten-free may contain gluten exceeding 20 ppm. The recall affects 4.6 million pounds distributed in the United States, Canada, Chile, Costa Rica, Guatemala, Mexico, and the United Kingdom.
Cargill is recalling PROSANTE TSOYFLR flour products nationwide and internationally due to potential gluten contamination in products labeled as gluten-free. The recalled products may contain gluten levels above 20 ppm.
Cargill is recalling PROSANTE vegetable protein bags labeled as gluten-free because they may contain gluten levels exceeding 20 ppm. Consumers with celiac disease or gluten sensitivity should not consume the affected product.
Cargill is recalling PROSANTE TSOYFLR flour products labeled gluten-free because they may contain gluten above 20 ppm. Consumers with celiac disease or gluten sensitivity should not consume these products.
Siemens ARTIS pheno angiography systems may misposition the C-arm by 5-10 millimeters when using the reference image positioning function, risking patient and staff crushing injuries. The device may also display inaccurate imaging overlays, potentially causing vessel perforation.
Inpeco laboratory automation systems' firmware can misassociate patient samples, potentially leading to incorrect electrolyte test results. The defect is rare but could cause serious medical consequences if results are misidentified or delayed.