State
72,933 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 72,933 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
Chrysler is recalling certain 2022–2026 Voyager and Pacifica vehicles because the right and left side curtain airbags may have insufficient pressure retention due to improperly sealed seams, increasing the risk of ejection and injury during a crash.
Sunnyyes LED mini lights are being recalled because the lithium coin batteries can be easily accessed by children, the remote battery compartment screw does not stay attached, and the packaging lacks required warnings.
DuraTrac is recalling stainless steel gas connectors sold between May and November 2025 because a manufacturing defect could cause a gas leak, posing a fire hazard.
MPINOI adult portable bed rails are being recalled because users can become entrapped within the rail or between the rail and mattress, and the rails lack the required hazard warning labels.
Petzl America is recalling Nomic and Ergonomic ice climbing axes because the shaft can break at the handle during use. Twenty-six shaft breakages have been reported, with no injuries.
Plunge Buddy is recalling DIY Sauna Heater Kits because electrical conductors within the kits can overheat. Twelve reports of overheating have been received, with no fires or injuries.
CCCEI power strips are being recalled because they do not contain supplementary overcurrent protection, creating a fire risk if overloaded. Two reports of sparking and melting have been received.
Volvo Trucks is recalling certain 2025-2026 VNL (4) vehicles because the service brake may take longer than expected to release, creating a crash risk and violating Federal Motor Vehicle Safety Standard 121.
Cardinal Health is recalling Webcol Alcohol Prep pads because of non-sterility, with microbial contamination identified as Paenibacillus phoenicis. The FDA has classified this recall as Class I.
Saputo Cheese USA is recalling Great Value Fat Free Cottage Cheese Small Curd due to potential under-pasteurization caused by a broken seal on the pasteurizer. The product was distributed to multiple states.
Saputo Cheese USA is recalling Great Value Cottage Cheese products because a broken pasteurizer seal may have resulted in underpasteurized product. The recall affects 16oz, 24oz, and 3lb containers distributed to multiple states.
Nissan is recalling 2026 Leaf vehicles because internal damage in the high voltage battery may cause a short circuit, increasing the risk of a fire.
Volvo Trucks is recalling certain 2025–2026 VNL (4) vehicles because the instrument panel may fail while driving, potentially hiding critical safety information like the speedometer and warning lights.
Strides Pharma is recalling two lots of Children's Ibuprofen Oral Suspension after complaints of a gel-like mass and black particles in the product.
Saputo Cheese USA is recalling Great Value Lowfat Cottage Cheese due to potential under-pasteurization caused by a broken pasteurizer seal. The product was distributed to ten states.
GE Medical Systems is recalling Centricity Universal Viewer software versions 7.0 through 7.0 SP2.0.1 because user login credentials may be exposed on the local client workstation.
ConvaTec is recalling two lots of the EsteemBody Drainable Pouch, REF 423643, because the drainable large pouch may leak due to a manufacturing issue.
GE Medical Systems is recalling Centricity Universal Viewer software versions 5.0 SP6 through 5.0 SP7.1 because user login credentials may be exposed on the local client workstation.
Diagnostica Stago is recalling the STA Liatest D-Di kit after investigations confirmed a positive bias in D-dimer measurements throughout the entire analytical range.
GE Medical Systems is recalling Centricity Universal Viewer software versions 6.0 through 6.0 SP10.4.1 because user login credentials may be exposed on the local client workstation.
Hologic is recalling one master lot of the Aptima HPV Assay because the product exhibits potential to generate either invalid or false negative results.
Apotex is recalling two lots of Brimonidine Tartrate/Timolol Maleate Ophthalmic Solution for lack of assurance of sterility.
Aston Martin is recalling certain 2025-2026 DBX and 2026 DBX S vehicles because the tire pressure monitoring system light may not illuminate to warn drivers of underinflated tires.
Baxter is recalling the Welch Allyn Spot Vision Screener VS100 on software version 3.2.0.1 because the display screen may unintentionally flicker, which may induce photosensitive seizure activity.
ConvaTec is recalling one lot of the EsteemBody Drainable Pouch, REF 423653, because the drainable large pouch may leak due to a manufacturing issue.