State
73,738 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 73,738 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
Mercedes-Benz is recalling 2018 S-Class and Maybach vehicles because improperly secured electrical power bars in the trunk may increase the risk of a fire or loss of vehicle functions.
Daimler Trucks North America is recalling 2018-2019 Freightliner Cascadia vehicles because brake caliper mounting bolts may not be properly tightened, potentially leading to reduced braking performance.
Daimler Trucks North America is recalling 2017-2018 Thomas Built Buses Saf-T-Liner EFX school buses because an incorrectly plumbed check valve may cause sudden parking brake activation and increase crash risk.
Mercedes-Benz is recalling 2018 GLA 250 vehicles because the center rear child seat tether anchor may be missing, preventing proper installation.
BMW is recalling 2017-2018 G310R and 2018 G310GS motorcycles because the side stand may damage the frame, causing the bike to fall over while stationary.
Dexter Ventline is recalling specific LP bottle straps because insufficient crimping may allow the buckle to detach. This could cause the propane tank to fall from the trailer, creating a road hazard.
General Motors is recalling 2016-2018 Chevrolet Malibu vehicles because the passenger presence system may be miscalibrated, potentially causing air bags to deploy incorrectly.
General Motors is recalling 2013 Chevrolet Volt vehicles because a software update may disable cell balancing, causing a low-voltage condition that could lead to a loss of propulsion and increased crash risk.
Grand Design is recalling 2018-2019 Solitude fifth-wheel trailers because the propane line may contact a hot grill, posing a fire risk.
Chrysler is recalling 2018 Dodge Journey vehicles because the rear camera view may not appear within two seconds of selecting reverse, increasing crash risk.
Chrysler is recalling 2017-2018 Pacifica vehicles because the Manual Park Release plug can be removed without a tool, violating federal safety standards.
Chrysler is recalling 2018 RAM 1500, 2500, 3500, and Dodge Journey vehicles because the backup camera may lose image display, increasing crash risk.
Lake Michigan Distilling is recalling 190 Proof Non-Denatured Grain Alcohol due to methanol contamination that could cause serious injury or death if consumed.
Draeger Medical Systems is recalling the Jaundice Meter JM-103 because users may misinterpret the out-of-range display as a zero measurement.
Hospira is recalling Naloxone Hydrochloride Injection cartridges due to the presence of particulate matter on the syringe plunger.
Volkswagen is recalling 2003 EuroVan, Jetta, Passat, and Golf vehicles because the driver's air bag inflator may explode during deployment, posing a risk of serious injury or death.
Porsche is recalling 715 Panamera vehicles because rear anti-roll bar links may detach, potentially affecting handling and increasing crash risk.
Draeger Medical Systems is recalling 6,711 Draeger Jaundice Meter JM-105 devices because users may misinterpret the out-of-range display as a zero measurement.
Ion Beam Applications is recalling 12C units due to an issue with the AdaPTinsight software used for patient localization in radiation therapy.
Tosoh Bioscience is recalling ST-AIA PACK CK-MB assays because Asfotase Alfa (Strensiq) interferes with the test, potentially causing inaccurate results.
Tosoh Bioscience Inc is recalling ST-AIA PACK C-Peptide assays because Asfotase Alfa (Strensiq) interferes with the test, potentially causing inaccurate results.
GE Healthcare is recalling 252 units of the Centricity Universal Viewer because image series may be missing from exams without a user warning.
Tosoh Bioscience is recalling ST-AIA PACK IGE II allergy assays because Asfotase Alfa (Strensiq) can cause inaccurate test results.
Tosoh Bioscience Inc is recalling AIA-PACK TSH 3rd Generation assays because Asfotase Alfa interferes with the tests, potentially causing inaccurate results.
Tosoh Bioscience is recalling ST-AIA PACK Myoglobin assays because the drug Strensiq interferes with the test, potentially causing inaccurate results.