State
72,936 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 72,936 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
Acme United Corporation is recalling WP WipesPlus Hand Sanitizing Wipes over current good manufacturing practice deviations.
Cipla USA is recalling three lots of Nilotinib Capsules 150 mg after out-of-specification results in description and visual appearance testing at six-month long-term stability.
Cipla USA is recalling one lot of Nilotinib Capsules 200 mg after out-of-specification results in description and visual appearance testing at six-month long-term stability.
Mercedes-Benz is recalling 2026 GLA 250 vehicles because an incorrectly installed bowden cable may prevent the door from opening from inside, potentially trapping occupants.
Kia is recalling certain 2026 K4 vehicles because the rear center seat belt anchor buckle may not latch properly, risking occupant restraint failure in a crash.
GM is recalling certain 2025-2026 Chevrolet Silverado 3500 and GMC Sierra 3500 vehicles with gasoline engines and dual fuel tanks because the rear fuel pump may not transfer adequate fuel to the front tank.
Forest River is recalling 2026 Dynamax Europa and Grand Sport GT motorhomes because the distribution panel may not be properly bonded to the chassis ground, posing a risk of injury or electrocution.
Toyota is recalling certain 2021-2024 Highlander and Highlander Hybrid vehicles because the second-row seat backs may fail to lock into position during seat back adjustment.
Webasto is recalling specific CV Standard Gen1 traction batteries that may fail, potentially causing loss of drive power or a fire.
General Motors is recalling 2025-2026 Chevrolet Express and GMC Savana cutaway vehicles because tires may have sidewall damage, increasing crash risk.
Escape Trailer Industries is recalling 2025 E17, E19, E21, and E5.0 recreational trailers because the spare tire carrier may detach during transit, creating a road hazard.
Mitsubishi Fuso is recalling 2024-2025 Rizon trucks because an electrical control unit error may prevent the vehicle from moving, increasing crash risk.
Forest River is recalling 2026 Impression fifth wheel trailers because exposed wire conductors may cause electrical arcing and increase fire risk.
HALO Magic Sleepsuits in three batch codes are being recalled because the zipper head can detach from the garment, posing a choking hazard to infants.
Forever 21 Kids Disney Mickey Mouse Pajama Pants are being recalled because they violate the mandatory flammability standards for children's sleepwear.
Tomum Minoxidil Hair Growth Treatment spray bottles are being recalled because the bottles are not child-resistant, as required for minoxidil under the Poison Prevention Packaging Act.
Pebble Mobility is recalling 2026 Flow recreational trailers because the adhesive securing roof solar panels may fail, creating a road hazard.
Cubimana Island Storm 3 In 1 Building Sets are being recalled because the battery compartment in the LED light piece lets children access button cell batteries.
Encore Medical, LP is recalling 14 EMPOWR 3D KNEE implants because they contain incorrect labeling. The recall affects US nationwide distribution.
Medline is recalling 8,773 NAIL KIT (Model DYKM1528) units because the sterile saline wound wash may not have been manufactured to the required sterility assurance level for sterile products.
Remel, Inc is recalling 97 units of Campy CVA Medium 100/PK, lot R01272, due to customer complaints reporting low to no recovery of Campylobacter Jejuni ATCC 33291. The product was distributed nationwide in AZ, CO, IL, NJ, OH, TN, and WA.
Prime Food Processing is recalling Dried Croaker Fish, 8 oz, because the fish is uneviscerated. The FDA has classified this recall as Class I, its most serious category.
Wizcure Pharmaa is recalling all lots of Fluorescein Sodium Ophthalmic Strips because the products may not have been manufactured according to current good manufacturing practices, raising concerns about sterility assurance.
Encore Medical, LP is recalling 20 Reverse Shoulder Prosthesis implants due to incorrect labeling. The recall affects nationwide distribution across multiple US states.
Agebox is recalling 665 bottles of iKids-Growth Day Formula capsules because they contain undeclared ibutamoren, a drug ingredient not approved for marketing in the U.S.