State
73,198 recalls have nationwide distribution and so reach Nevada. 5,696 additional recalls listed Nevada specifically in their distribution scope.
Of the 5,696 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 1,479 (26%) are Severe.
Which agencies issued them
These figures cover only the 5,696 recalls whose distribution notice names Nevada specifically. The 73,198 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
USDA FSIS issued a public health alert for Whole Foods Market Kitchens soup mislabeled as beef, containing undeclared sesame.
Moonsea Pack and Play Mattresses sold on Amazon violate federal crib mattress safety regulations and pose a suffocation hazard to infants. Consumers should stop using them immediately and contact Moonseasleep for a refund.
Adven Group LLC is recalling about 1,540 Nap Queen 12-inch Maxima Hybrid Mattresses sold via Amazon, Walmart, and Overstock because they fail to meet federal flammability standards and pose a fire hazard.
Pilotcar is recalling 265 vehicles from 2021-2023 because the rearview camera and monitor were not installed, reducing rear visibility and increasing crash risk.
Volkswagen is recalling certain 2023-2024 ID.4 vehicles because the panoramic sunshade may not be fire retardant enough, violating federal safety standards.
Sumitomo is recalling specific Falken Wildpeak tires because a manufacturing error may cause sidewall punctures and air leaks, increasing crash risk.
SourceOne Ventures recalls Windsor Queen Xtrabed Mobile Murphy Beds due to risks of cabinet breakage and tip-over. About 12,000 units sold at Wayfair between November 2016 and April 2023 are affected.
Pilotcar is recalling 265 low-speed electric vehicles because they lack the required pedestrian warning sound system, increasing the risk of crashes.
Bugaboo is recalling about 1,000 Dragonfly Seat Strollers because the backrest can move downward in parent-facing mode, causing unrestrained infants to potentially tumble from the seat. No U.S. injuries have been reported.
Bunkhouse and Lotsa LITES! Connectable Mini String Lights can overheat and present burn and fire hazards when plugged directly into an outlet. About 34,600 units are affected.
The electric cord plug prong on Oreck Discover Upright Vacuums can detach and remain in electrical outlets, creating an electrical shock hazard. About 6,200 units sold nationwide from September 2022 through September 2023 are affected.
Ergodyne is recalling about 16,570 Squids 3705 Wire Tool Attachments because the wire can break when dropped while tethering a tool over two pounds, posing an injury risk to bystanders below.
Garland Ventures is recalling 13,842 pounds of ready-to-eat chicken fried rice products that may be contaminated with Listeria monocytogenes.
Botanical Be is recalling Kuka Flex Forte caplets nationwide because they contain undeclared diclofenac and were marketed without required FDA approval. All lots expire 12/12/2024.
Bayer Healthcare Pharmaceuticals Inc. is recalling 192 bottles of VITRAKVI (larotrectinib) oral solution due to microbial contamination identified as Penicillium brevicompactum during routine testing.
BMW is recalling certain 2023 models with a transmission control unit weld defect that may allow oil leakage, risking sudden power loss and increased crash risk.
Botanical Be is recalling 235 bottles of Artri King tablets sold nationwide. The tablets contain undeclared diclofenac and were marketed without FDA drug approval.
Reumo Flex caplets packaged in 30-count boxes are being recalled because they contain undeclared diclofenac and were marketed without FDA approval. The product was distributed nationwide.
Apotex Corp. is recalling Paroxetine 10 mg tablets nationwide due to out-of-specification impurities in an excipient. Affected lots expire 08/2024.
Glenmark Pharmaceuticals is recalling Naproxen Sodium 250mg tablets nationwide due to a labeling mix-up where Indomethacin bottles may be labeled as Naproxen. Patients could receive the wrong medication.
Paroxetine tablets are being recalled for failing specification tests due to higher-than-acceptable levels of a degradation impurity. Approximately 1,941 bottles distributed nationwide are affected.
Breas Medical is recalling 215 mouthpiece units due to manufacturing defects with unintended slits that may result in insufficient ventilation in mechanical ventilation patients.
Apotex Corp. is recalling nationwide 25,776 units of Paroxetine Hydrochloride 30 mg tablets due to out-of-specification impurities. Affected lot numbers RV8686, RX0119, and RV2254 expire 08/2024.
Apotex Corp. is recalling Paroxetine Hydrochloride 40 mg tablets nationwide due to failed quality specifications. Testing found out-of-specification impurity levels in affected lot numbers.
Kovatch Mobile Equipment is recalling 2020 Severe Service, Predator, and Spartan MetroStar trucks because a firmware defect may cause electrical fires.