State
73,388 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 73,388 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
Ford is recalling 2022 Transit vehicles because the rearview camera may display a blank image when reversing, increasing crash risk.
Ford is recalling 2022 F-150 and related models due to a software error that may disable trailer brake functionality. Loss of trailer brakes increases stopping distance and crash risk.
Boxine US is recalling tonies Blocks wooden toys containing high-powered magnets sold online from November through December 2021. When swallowed, multiple magnets can lodge in the digestive system and cause serious injury or death.
Prevost is recalling 140 X3-45 Commuter buses from 2021-2022 because a loose cable in the rear junction box may overheat and cause a fire.
EGL Motor is recalling about 500 EGL and ACE-branded youth ATVs (models MADIX 110 and B125) sold nationwide from May to September 2020 due to violations of federal ATV safety standards. The vehicles exceed speed limits for their age group, have defective brakes, and handlebars that pose laceration hazards in crashes.
Chrysler is recalling 2021-2022 Pacifica and 2021 Voyager vehicles because the second-row seat mounting latch may fail to secure the seat properly, increasing the risk of injury in a crash.
Commencal Ramones 14-inch children's bicycles lack required foot brakes and are equipped only with hand brakes, posing a crash hazard or risk of injury to young children unable to stop them. About 925 bicycles are affected.
Segway is recalling about 960 Ninebot children's bicycle helmets because they fail to meet safety standards for positional stability and retention, creating a risk of head injury in a crash. No injuries have been reported.
Sakar International is recalling about 89,000 Dimensions Bluetooth Speaker Helmets sold at Walmart because they do not meet U.S. federal safety standards for bicycle helmets and pose a risk of head injury in a fall.
Reading Truck is recalling 2019-2021 Master Mechanic Crane vehicles because a poorly mounted module can overheat and cause a fire.
Certain 2021-2022 Jeep Grand Cherokee L vehicles may have a missing weld in the child seat tether anchorage system. This could allow the tether to separate during a crash, increasing the risk of child injury.
Audi is recalling 2013-2017 A8, S6, S7, S8, and RS7 vehicles because a blocked turbocharger oil strainer can cause engine failure and increase crash risk.
Volkswagen is recalling certain 2022 and 2021 vehicles because rear suspension knuckles may corrode, crack, and break, potentially causing loss of stability and increasing crash risk.
B. Braun Medical, Inc. is recalling 33,742 bags of 0.9% Sodium Chloride Injection USP due to leaking that compromises sterility assurance. The intravenous medication was distributed nationwide.
Jaguar Power Honey packaged in gold boxes is being recalled nationwide because it contains a hidden drug ingredient not listed on the label. Consumers should not consume this product.
SD Biosensor's STANDARD Q COVID-19 Ag Home Test kits were illegally imported without FDA approval, clearance, or authorization. Approximately 400,000 units were distributed nationwide.
Walmart is recalling Avaphinal Maximum Male Enhancement Sexual Pills (2000 MG, 10-capsule cartons, Lot DK1027) distributed nationwide because they contain undeclared sildenafil, making them an unapproved drug.
Helmi Honey VIP is being recalled nationwide due to the presence of an undisclosed drug ingredient. Consumers should stop using the product and return it.
Boston Scientific is recalling RX CHOLANGIOGRAM KIT due to a sterile barrier breach that compromises device sterility. Approximately 500 units distributed worldwide are affected.
Boston Scientific Corporation is recalling 1,811 units of Dreamtome Cannulating Sphincterotomes worldwide because the sterile barrier is compromised, creating a potential contamination risk.
Boston Scientific is recalling 142 units of DREAMTOME 44-30MM/450CM medical devices distributed worldwide due to a sterile barrier breach that compromises device sterility. Affected lot numbers are 27625066 and 27805561.
Hill-Rom Traverse Rail Carrier E-System components contain non-conforming screws that are too short to secure the rail properly. The screws could loosen over time, causing the rail system to fall and potentially injure caregivers or patients.
GE Healthcare is recalling 10,445 CARESCAPE Central Station monitoring systems. If connected to an unapproved keyboard, audio alarms may be muted, potentially preventing users from receiving critical notifications.
Boston Scientific is recalling 14 JAGTOME RX medical devices worldwide due to a sterile barrier breach that compromises the device's sterility.
Bard Peripheral Vascular Inc is recalling 1,260 Adult Lumbar Puncture Drug Free Trays due to manometer leaking and mating issues that could affect device function.