State
72,919 recalls have nationwide distribution and so reach Virginia. 9,479 additional recalls listed Virginia specifically in their distribution scope.
Of the 9,479 recalls naming Virginia we have scored against our rubric, 1,285 (14%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 2,294 (24%) are Severe.
Which agencies issued them
These figures cover only the 9,479 recalls whose distribution notice names Virginia specifically. The 72,919 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
Sanlebi Pet Vet Playsets are recalled because the button cell batteries in the nail grinder and otoscope can be easily accessed by children. About 4,650 units are affected.
Certain Generac portable generators are recalled because fuel can leak from the carburetor when the generator is first filled with gasoline. 114 fuel leak reports have been received; no injuries.
Sweetcrispy electric pressure washers are recalled because they lack an integral ground-fault circuit interrupter, posing shock and electrocution hazards. 2,300 units are affected.
Agiiman pressure washers are recalled because they lack an integral ground-fault circuit interrupter, posing shock and electrocution hazards. 80 units are affected.
ATOYUS wooden activity cubes are recalled because the xylophone screws and clock hands can detach, violating the small parts ban for toys intended for children under three.
Manik and Apex-branded ATX computer power supplies are recalled because they lack a permanent on-product label warning of shock and electrocution hazards if the unit is opened.
Medline is recalling Non Vascular Pack and Vein convenience kits containing NAMIC rotating adaptor control syringes because the adaptor can unwind and disconnect during use.
Audi is recalling certain 2019-2024 e-tron and Q8 e-tron vehicles because an improperly assembled fastener can cause the brake pedal to detach from the brake booster.
Medline is recalling Shoulder Arthroscopy and Extremity Pack convenience kits containing NAMIC rotating adaptor control syringes because the adaptor can unwind and disconnect during use.
Medline is recalling Minor Plastic-LF convenience kits containing NAMIC rotating adaptor control syringes because the adaptor can unwind during use and disconnect from the manifold.
Medline is recalling right and left heart catheterization and angiography kits containing NAMIC rotating adaptor control syringes because the adaptor can unwind and disconnect. 79,843 units are affected.
Roush is recalling 1,217 2026 Nissan Frontier Pro4X R vehicles because steering and suspension fasteners may be loose or missing, posing a crash risk.
Medline is recalling a further group of NAMIC Angiographic Syringe lots because the rotating adaptor can unwind during use and disconnect from the manifold. 149,439 units are affected.
Medline is recalling Delivery Pack convenience kits containing NAMIC rotating adaptor control syringes because the adaptor can unwind during use and disconnect from the manifold.
Medline is recalling Head and Neck CDS-LF and Heart Cath Pack-LF convenience kits containing NAMIC rotating adaptor control syringes because the adaptor can unwind and disconnect.
Medline is recalling Robotic Pack and Uro/Gen Robotic Pack convenience kits containing NAMIC rotating adaptor control syringes because the adaptor can unwind and disconnect during use.
Medline is recalling cath lab and angiography procedure packs containing NAMIC rotating adaptor control syringes because the adaptor can unwind and disconnect. 17,902 kits are affected.
Medline is recalling TAVR PACK convenience kits containing NAMIC rotating adaptor control syringes because the adaptor can unwind during use and disconnect from the manifold. 108 units are affected.
Medline is recalling NAMIC Angiographic Syringes across multiple sizes because the rotating adaptor can unwind during use and disconnect from the manifold. 1,752,096 units are affected.
Medline is recalling Angio Pack and Neuro Interventional Radiology convenience kits containing NAMIC rotating adaptor control syringes because the adaptor can unwind and disconnect during use.
Medline is recalling CVOR Angiography Pack-LF convenience kits containing NAMIC rotating adaptor control syringes because the adaptor can unwind and disconnect during use. 3,120 kits are affected.
Medline is recalling GLOVE PACK 7.0 convenience kits containing NAMIC rotating adaptor control syringes because the adaptor can unwind during use and disconnect from the manifold.
Medline is recalling Special Procedure Trays containing NAMIC rotating adaptor control syringes because the adaptor can unwind during use and disconnect from the manifold. 762 units are affected.
Medline is recalling a further tranche of NAMIC Angiographic Syringes because the rotating adaptor can unwind during use and disconnect from the manifold. 2,630,369 units are affected.
Medline is recalling NAMIC Angiographic Control Syringes because the rotating adaptor can unwind during use, causing a loose connection or full disconnection from the manifold. 192,690 units are affected.