State
73,737 recalls have nationwide distribution and so reach US Virgin Islands. 178 additional recalls listed US Virgin Islands specifically in their distribution scope.
Of the 178 recalls naming US Virgin Islands we have scored against our rubric, 12 (7%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 39 (22%) are Severe.
Which agencies issued them
These figures cover only the 178 recalls whose distribution notice names US Virgin Islands specifically. The 73,737 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
General Motors is recalling 2019 Buick Encore, Chevrolet Spark, Traverse, and Trax vehicles because the air bag module may not be programmed correctly, preventing deployment in a crash.
Ford is recalling specific 2010-2012 vehicles to replace passenger air bag modules that may fail to inflate properly in a crash.
Honda is recalling specific 2016-2019 HR-V, Odyssey, and Acura MDX models because rear brake caliper pistons may have insufficient coating, reducing braking performance.
Mack Trucks is recalling 2019 Anthem, Granite, and Pinnacle vehicles because a loose pinch bolt may allow the steering shaft to separate, causing loss of steering.
Toyota is recalling 2004-2006 Scion xA vehicles because the air bag control module may short, causing air bags to deploy unintentionally or fail to work.
Subaru is recalling 2018 Legacy and Outback vehicles because a software error may cause the fuel gauge to display incorrect levels, increasing the risk of stalling and a crash.
Subaru and Toyota are recalling specific 2012-2014 Impreza, BRZ, XV Crosstrek, and FR-S models because engine valve springs may fracture, potentially causing an engine stall that increases crash risk.
Black & Decker is recalling specific hammer drills and drill drivers because the side handles can slip or break, posing an injury risk.
Pain Relief Naturally is recalling lidocaine creams, sprays, and gels because the packaging failed to meet child-resistant closure requirements, posing a poisoning risk to young children.
MCS Industries is recalling about 15,400 Glacier Bay bi-view medicine cabinets sold at The Home Depot because the mirror can detach and break, posing a laceration hazard.
Alcon is recalling the CyPass Micro-Stent implant because long-term study data showed statistically significant endothelial cell loss in patients who received the device.
Alcon Research is recalling the CyPass Micro-Stent because long-term study data showed statistically significant endothelial cell loss in patients who received the device.
Upsher Smith is recalling Bumetanide tablets because the product failed impurity specifications for an unspecified degradation product.
Forest River is recalling 2018-2019 Berkshire RVs and StarTrans/Glaval buses because brake caliper mounting bolts may be insufficiently tightened, increasing crash risk.
GE Medical Systems is recalling four Signa Architect MRI scanners because a small area on the bore surface can get warm enough to cause a serious burn if proper padding is not used.
Heritage Pharmaceuticals is recalling Cidofovir Dihydrate Injection due to complaints of dried powder on the outside of the bottle, which raises concerns about the product's sterility.
Westlab Pharmacy is recalling 222 syringes of ADAA Cataract Drops nationwide due to a lack of process controls.
Bovie Medical Corporation is recalling J-Plasma Precise 360 handpieces because the PEEK tip may separate and remain in patient tissue.
Westlab Pharmacy is recalling Cyclosporine 1% Human Eye Drops due to a lack of process controls. The recall covers nationwide distribution.
Suzuki is recalling 2010-2013 Kizashi vehicles because dust in the vent line may crack the fuel tank, increasing the risk of a fuel leak and fire.
Alcon is recalling the CyPass Micro-Stent implant because long-term study data showed statistically significant endothelial cell loss in patients.
Pfizer is recalling 71,075 vials of Meropenem for Injection because the containers may have lost integrity, compromising sterility.
Alcon Research is recalling CyPass Micro-Stent devices because long-term study data showed statistically significant endothelial cell loss in patients.
ESAOTE S.P.A. is recalling 10 MyLab Gamma, Model 7410 ultrasound systems because probe power monitoring settings may cause the probe head to overheat during continuous operation.
Keystone RV Company is recalling 2019 Crossroads Cruiser recreational trailers because the water heater exhaust may allow carbon monoxide or propane gas to enter the living quarters.