State
72,969 recalls have nationwide distribution and so reach Nevada. 5,692 additional recalls listed Nevada specifically in their distribution scope.
Of the 5,692 recalls naming Nevada we have scored against our rubric, 951 (17%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 1,476 (26%) are Severe.
Which agencies issued them
These figures cover only the 5,692 recalls whose distribution notice names Nevada specifically. The 72,969 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
Endosee System Convenience Kits with IV Tube are being recalled because they contain non-sterile iodine pouches while the peel away lid labels incorrectly identify them as sterile. 475 units affected.
The Azurion 7 M20 fluoroscopic x-ray system is being recalled because of the potential for bolts connecting the gearbox to the mounting flange of the C-arm to become loose. 78 units affected.
Medtronic CareLink SmartSync Device Manager is being updated because in prior application versions the abort window during an induction test limited the user's ability to cancel high voltage therapy. 22,091 devices affected.
Ritz Cracker Sandwiches 20 count variety packs are being recalled because of undeclared peanut allergens due to mispackaging. 13,872 cases are affected.
Epinephrine Lidocaine HCl 0.25 mg/mL and 7.5 mg/mL vials compounded by Imprimis NJOF are being recalled because of subpotent assay results during stability testing. 6,880 vials affected.
BD COR System Software version 8.80 and above is being recalled because of a potential functionality issue supporting the Over labeling feature that could lead to possible false negative results. 7 systems affected.
Budesonide Inhalation Suspension 0.5 mg/2 mL is being recalled for lack of assurance of sterility after a market complaint was received for leakage and an empty ampoule. 13,680 ampoules affected.
Endosee System Convenience Kits are being recalled because they contain non-sterile iodine pouches while the peel away lid labels incorrectly identify them as sterile. 991 units are affected.
Brinkley RV is recalling certain 2025 Model Z trailers because the electrical wiring may not be secured properly, which can damage the wiring and cause a short circuit.
HSG Procedure Trays are being recalled because they contain non-sterile iodine pouches while the peel away lid labels incorrectly identify them as sterile. 171 units are affected.
The Covidien Nellcor Bedside SpO2 Patient Monitoring System is being recalled because alarms may not be heard or recognized, which the manufacturer links to treatment delay. 264,790 units are affected.
A compounded Tropicamide-Proparacaine-Phenylephrine-Ketorolac sterile ophthalmic solution is being recalled because of subpotent assay results during stability testing. 2,890 vials are affected.
Clomipramine Hydrochloride Capsules USP 25 mg are being recalled after an out of specification result for an unspecified degradation product during retention sample testing at expiry. 2,724 bottles affected.
Sushi Wasabi 5 gram ready to eat mini packs are being recalled because the individual consumer size label does not declare the ingredient Yellow 5. 1,848 cases are affected.
ACUVUE OASYS MAX 1-Day MULTIFOCAL contact lenses are being recalled because of defects, specifically bubbles and voids, identified during standard finished goods testing. 114,165 lenses affected.
Terran Industries is recalling 7000lb axle assemblies because incorrect suspension components may have been installed, posing a risk of axle spring failure or wheel detachment.
Mack Trucks is recalling 2026 Granite GR trucks because incompatible brake drums and steer axles may cause loss of brake function, increasing crash risk.
Kia is recalling certain 2023-2025 Telluride vehicles because the door belt molding trim can delaminate and detach from the vehicle, becoming a road hazard.
Kia is recalling certain 2023-2025 K5 vehicles because the left and right rear window trim pieces may loosen and detach, becoming a road hazard for other vehicles.
Porsche is recalling 2024-2025 Macan 4 Electric vehicles because front seat air bags may be improperly secured, potentially preventing proper deployment during a crash.
Grech Motors is recalling certain 2020-2025 Strada, Turismo and Terreno motorhomes because the retractable awning may extend unintentionally while the vehicle is moving.
Tesla is recalling certain 2026 Model Y vehicles because the horn ground wire ring terminal may be improperly secured, causing the horn to fail. An inoperable horn increases the risk of crashes.
USDA FSIS issued a public health alert for Reser's and Molly's Kitchen ham salad products containing breadcrumbs recalled for possible Listeria monocytogenes contamination.
Mercedes-Benz is recalling certain 2022-2023 EQB 300 and EQB 350 4MATIC vehicles because the high voltage battery bus bar may be secured with incorrect screws, causing a sudden loss of drive power.
Ford is recalling certain 2025 Lincoln Navigator, F-150, Expedition, Bronco and Ranger vehicles because the Electronic Brake Booster module may malfunction, causing a loss of power brake assist.