State
72,986 recalls have nationwide distribution and so reach Virginia. 9,483 additional recalls listed Virginia specifically in their distribution scope.
Of the 9,483 recalls naming Virginia we have scored against our rubric, 1,286 (14%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 2,296 (24%) are Severe.
Which agencies issued them
These figures cover only the 9,483 recalls whose distribution notice names Virginia specifically. The 72,986 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
Lamborghini is recalling 2024-2025 Revuelto vehicles because gas springs may fail, causing doors to close unexpectedly and increasing injury risk.
Above-ground pools 48 inches and taller with compression straps over the vertical support legs are being recalled because the strap can create a foothold. CPSC believes nine children have drowned.
Rosenbauer America is recalling 2019-2024 fire trucks because a software error may cause the odometer to freeze, potentially delaying critical safety maintenance.
CasaClean Handheld Steamers, model DF-958, are being recalled because they can leak steam or spew hot boiling water. Thirteen consumers have received burns. About 23,000 units are affected.
iStore Magnetic Wireless Power Banks, model IST-09991/W05, are being recalled because the lithium-ion battery can overheat and ignite while charging. Three incidents and about $15,000 in property damage reported.
Traveller aluminum loading ramps are being recalled because they cannot withstand the weight specified on the ramps and can bend or break in use. Two injuries have been reported. About 18,000 units affected.
36-volt lithium-ion batteries supplied with certain VIVI e-bikes are being recalled because they can overheat. Fourteen overheating incidents including three fires have been reported. About 24,000 units affected.
Kayem Foods is recalling ready-to-eat chicken sausage products nationwide due to possible contamination with pieces of plastic.
Grand Design is recalling certain 2025-2026 Lineage trailers with Lippert Modularia entrance doors because the door latch mechanism may fail, potentially trapping occupants in an emergency.
Chrysler is recalling certain 2024-2025 Pacifica vehicles that were built with an incorrect radio, which can prevent the rearview camera image displaying. All affected vehicles have been repaired.
Chrysler is recalling Mopar second-row head restraints that may not lock in the upright position, increasing injury risk during a crash.
Chrysler is recalling certain 2023-2024 Jeep Grand Cherokee and Grand Cherokee L vehicles because the second-row head restraints may not lock in the upright position, failing FMVSS 202.
Primark DTR Stitch Scented Highlighters 4-packs are being recalled because they contain phthalates in violation of the federal phthalates ban. About 2,600 units are affected.
Babyletto Kiwi Electronic Recliner and Swivel Gliders are being recalled because the USB module in the recliner arm can overheat and spark. About 9,030 units are affected.
Hyundai is recalling certain 2023-2025 Genesis G90 and GV60 vehicles because a software error may cause the instrument panel display to fail, failing FMVSS 101.
Centropneus is recalling 640 Michelin CrossClimate 2 tires because they are missing the required DOT certification symbol on the sidewalls.
Weaver Chocolates Nonpareil Semi-Sweet Chocolate in 25 lb bulk cases is being recalled because of an undeclared milk allergen. 849 cases are affected.
Edwards FEM-FLEX II Femoral Arterial Cannulas, model FEMII016A, are being recalled after complaints of a 3 mm to 4 mm section of wire exposed or protruding from the cannula body. 6,801 units affected.
Edwards FEM-FLEX II Femoral Arterial Cannulas, model FEMII018AS, are being recalled after complaints of a 3 mm to 4 mm section of wire exposed or protruding from the cannula body. 558 units affected.
BMW is recalling certain 2022-2025 iX, 2023-2024 i7 and 2022-2023 i4 vehicles because high-voltage battery cell modules may not have been assembled properly, stressing the module frame.
Edwards FEM-FLEX II Femoral Arterial Cannulas are being recalled after complaints of a 3 mm to 4 mm section of wire exposed or protruding from the outside of the cannula body. 847 units affected.
Edwards Optisite OPTI16 Arterial Cannulas are being recalled after complaints of a 3 mm to 4 mm section of wire exposed or protruding from the outside of the cannula body. 27,022 units affected.
Edwards Optisite OPTI18 Arterial Cannulas are being recalled after complaints of a 3 mm to 4 mm section of wire exposed or protruding from the outside of the cannula body. 13,240 units affected.
The Bravo CF capsule delivery device is being recalled because misapplied adhesive may prevent the pH capsule attaching to the oesophagus or detaching from the delivery device. 128,202 units affected.
Edwards FEM-FLEX II Femoral Arterial Cannulas, model FEMII018A, are being recalled after complaints of a 3 mm to 4 mm section of wire exposed or protruding from the cannula body. 13,240 units affected.