State
73,503 recalls have nationwide distribution and so reach US Virgin Islands. 177 additional recalls listed US Virgin Islands specifically in their distribution scope.
Of the 177 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 177 recalls whose distribution notice names US Virgin Islands specifically. The 73,503 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
Altec is recalling 2005-2021 aerial devices because boom spools can shift, increasing injury risk. Owners should contact Altec for free repairs.
Custom Truck is recalling 2020 Ford F-550 vehicles because LCD displays may lock up, potentially delaying emergency efforts.
Ford is recalling 2021 F-150 vehicles because internal steering gear damage could cause loss of steering control. Owners should not drive until the repair is complete.
Mercedes-Benz USA is recalling approximately 218 2021 Cabriolet models due to rear headrests that may be incorrectly mounted to the seatbacks. The headrests could move or detach during a crash, increasing the risk of injury.
Mercedes-Benz is recalling 2020 GLB 250 vehicles because water may enter the foot wells, potentially causing electrical damage, engine stalls, or a blank instrument cluster.
Mercedes-Benz is recalling 2020 GLB 250 vehicles because the front passenger air bag may tear upon deployment, increasing injury risk.
Mercedes-Benz is recalling 2020 GLB 250 vehicles because side curtain air bags may not deploy properly in a crash, increasing injury risk.
BMW is recalling 1999-2001 3 Series vehicles because the driver-side air bag inflator may explode or underinflate, posing a risk of serious injury.
Nissan recalls 2021 INFINITI QX50 and other vehicles due to front steering knuckles and rear axle housings with insufficient strength from improper heat treatment, which could deform on impact and cause loss of steering control or wheel separation.
Triple E Recreational Vehicles is recalling 2020-2021 Serenity, Unity, and Wonder models because a low-positioned metal deflector allows exhaust to char the wood frame, increasing fire risk.
Chrysler is recalling RAM trucks because incorrect manual torque specifications can cause wheel studs to over-tighten, break, and lead to wheel separation and possible crashes.
Umbrosa is recalling about 250 pool and patio umbrellas because the arm can break at the elbow while in use, posing an injury hazard.
Williams Advanced Materials & Chemicals is recalling sodium hydroxide, heptane, and naphtha because the packaging is not child-resistant and labels violate federal requirements.
Temsa is recalling 276 vehicles because a sealing washer defect may cause high-pressure fuel leaks, increasing the risk of fire.
Simkins Brothers Sweets is recalling Natural Way Almond Butter due to potential undeclared peanuts. Consumers should check for lot #505721.
Biopsybell S.R.L. is recalling 250 units of 10 Gauge Cement Delivery Cannulas labeled as sterile but potentially not sterilized.
Daimler Trucks North America is recalling 2019 Freightliner M2 Business Class vehicles with 14Xe ePowertrains because insufficiently crimped stator wires may cause overheating and loss of drive power.
Biopsybell is recalling 160 units of 11G Direct Single Delivery kits because they were labeled as sterile but may not have been sterilized.
Teva Pharmaceuticals is recalling Methylprednisolone Acetate Injectable Suspension due to a lack of assurance of sterility.
Biopsybell is recalling 50 units of 11G Direct Single Access devices labeled as sterile but potentially not sterilized, distributed in Mississippi and Kentucky.
Teva Pharmaceuticals is recalling specific lots of Haloperidol Decanoate Injection because the company cannot guarantee the product is sterile.
Thor Motor Coach is recalling certain 2022 Sequence, Rize, Scope, and Tellaro recreational vehicles. The Flex-190 solar panel junction box may experience electrical shorts, increasing the fire risk.
Hyobin LLC is recalling Triple SupremeZen Plus 3500 capsules because FDA analysis found the unapproved drug tadalafil. The product was marketed without an approved NDA or ANDA.
Hyobin LLC is recalling PremierZen Black 5000 capsules because FDA analysis detected the unapproved drug tadalafil. The product was marketed without an approved NDA or ANDA.
Biopsybell S.R.L. is recalling 625 units of 10 Gauge Direct Unilateral Stylets because they were labeled as sterile but may not have been sterilized.