State
72,907 recalls have nationwide distribution and so reach West Virginia. 3,541 additional recalls listed West Virginia specifically in their distribution scope.
Of the 3,541 recalls naming West Virginia we have scored against our rubric, 593 (17%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 657 (19%) are Severe.
Which agencies issued them
These figures cover only the 3,541 recalls whose distribution notice names West Virginia specifically. The 72,907 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
Piaggio is recalling 2026 Liberty 50 and 150 motorcycles because a circuit fault may cause headlights to turn off, increasing crash risk.
Farber Specialty is recalling 2025-2026 HX620 and MCXCR emergency vehicles because the touchscreen may fail, preventing the activation of exterior lights and emergency equipment.
General Motors is recalling 2026–2027 Cadillac Vistiq vehicles because the third-row power seatback may fail to reverse when it encounters a person, potentially trapping them.
About 1,060 Pyro Diablo "Diablo Rising" 9 Shots fireworks devices are being recalled because their pyrotechnic composition exceeds the federal limit.
About 2,200 BABESIDE doll and stroller toy sets are being recalled because the small pacifier violates the small parts ban and the plush bear's eyes can detach.
Toyota Motor Engineering & Manufacturing is recalling 2026 Subaru Solterra vehicles due to a fault in the battery electronic control unit that may cause loss of drive power, increasing crash risk.
Veseacky children's pajama sets are recalled due to burn hazards from violating mandatory safety standards for children's sleepwear. About 3,700 units were sold on Amazon from October 2020 through January 2026.
About 2,355 CooCooBaby Classic and Deluxe Baby Loungers are being recalled for violating the mandatory standard for infant sleep products, posing a suffocation hazard.
SHEIN Distribution Corporation is recalling about 160 Michley children's pajamas that violate the mandatory flammability standard for children's sleepwear, posing a burn injury or death risk. No injuries have been reported.
About 3,840 Joolz Aer2 Car Seat Adapters are being recalled because they can fail to attach properly to the stroller, which may allow the car seat to fall.
About 5,000 Arizer Solo III Intergalactic (Black) portable vaporizers are being recalled after four reports of the internal lithium-ion battery exploding or igniting.
TNVitamins and Doctor's Pride moringa green superfood capsules are being recalled because the product may be contaminated with Salmonella. 13,000 bottles are affected.
Doxorubicin Hydrochloride Liposome Injection, 50 mg/25 mL single-dose vials, is being recalled because of particulate matter identified as glass. 675 vials are affected.
Beekeeper's Naturals Saline Nasal Spray with propolis and xylitol, 1 fl oz, is being recalled for microbial contamination of non-sterile products. 1,680 bottles are affected.
Gas-X Extra Strength simethicone 125 mg softgels are being recalled because of contamination with a diluted propylene glycol-based coolant leaked from a machine during packaging.
Bicarby Dialysate across six model numbers is being recalled because luer-lock leaks during preparation present a potential slip and fall hazard from fluid on the floor.
Allia IGS Pulse angiographic X-ray systems are being recalled because an electrical cable issue could expose service personnel to electrical shock while power is on.
Plum Duo Precision IV Pumps are being recalled because under certain conditions the pump may not display a soft limit alert before delivery starts, potentially leading to under- or over-delivery.
MIC Safety PEG Kits, 20 Fr PUSH OTW, catalog number 7170-20, are being recalled because they contain lidocaine hydrochloride injection subject to a supplier recall. 901 kits affected.
Merlin Patient Care System programmer software is being recalled because a malfunction during a pacing capture threshold test may stop the command to terminate the test being communicated.
CGuard Prime Carotid Stent Systems, 135 cm with an 8 mm x 30 mm stent, are being recalled because the delivery system may meet high resistance or fail to deploy the stent.
Park St. Deli Macaroni & Cheese, 20 oz, is being recalled because of undeclared soy lecithin. The action covers 58,405 cases.
MIC Safety PEG Kits, 20 Fr PULL, catalog number 7180-20, are being recalled because they contain lidocaine hydrochloride injection subject to a supplier recall. 3,184 kits affected.
Boston Scientific is removing Orca Sterile, Single Use Air/Water and Suction Valves because of a higher than anticipated occurrence of the suction button sticking. 9,750 units affected.
Budesonide Inhalation Suspension, 1 mg/2 mL single-dose ampules from Sun Pharmaceutical, is being recalled after a quality complaint of black or brown specs and particles in the solution.