State
73,096 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 30 (17%) are Severe.
Which agencies issued them
These figures cover only the 177 recalls whose distribution notice names US Virgin Islands specifically. The 73,096 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
Certain 2023 Jeep Grand Cherokee vehicles have a loose second-row seat belt buckle bolt that may not properly restrain occupants during a crash. Dealers will inspect and tighten the bolt free of charge.
Retrospec is recalling about 530 Beaumont Plus ST bicycles with disc brakes because the front brake rotor and pads can become misaligned, potentially causing brake failure and crashes. No injuries have been reported.
Daikin Comfort Technologies Manufacturing is recalling about 12,100 Amana, Daikin, and Goodman branded air conditioning and heat pump packaged units due to incorrect electrical ratings on the serial plate that could lead to improper wiring and fire risk.
Bambu Lab is recalling about 12,800 A1 3D printers sold between December 2023 and January 2024 due to damaged or bent heatbed cables that can short-circuit, spark, or burn through insulation, creating electric shock and fire risks. No injuries have been reported.
Adven Group is recalling approximately 117,200 Nap Queen Sleep Victoria Hybrid Mattresses sold nationwide from February 2020 through October 2023 because they violate federal flammability regulations, posing a fire hazard.
Black Diamond Equipment is recalling Neve Strap Crampons and Accessory Kits because screws connecting the heel cup to the crampon can loosen, causing the heel cup to detach and creating a fall hazard. The firm has received three reports of incidents but no injuries have been reported.
Altec is recalling 2023-2024 aerial devices and related truck-mounted equipment due to lighting wire harness overload that may prevent vehicle lights from illuminating, reducing visibility to other drivers and increasing the risk of crashes.
Airstream is recalling 2024 Interstate motorhomes because a missing 12-volt fuse could allow the supply wire to overheat, increasing the risk of fire.
Megadyne Medical Products is recalling its MEGA SOFT Pediatric Patient Return Electrode due to reports of patient burns during electrosurgical use. Approximately 1,270 units distributed worldwide are affected.
Endera is recalling 2021-2024 school buses because seat assemblies may lack reinforcing washers, causing non-compliance with safety standards and increasing injury risk.
PACCAR is recalling 2025 Kenworth and Peterbilt trucks due to improperly heat-treated ball studs in steering assemblies that may break, causing loss of steering control.
Forest River is recalling 3,192 school buses because the restraining barrier may not provide sufficient protection in a crash, increasing injury risk.
Arrow International is recalling intra-aortic balloon catheter kits due to potential inflation failure, catheter damage, and helium loss that could cause serious health consequences.
Arrow International is recalling its UltraFlex Intra-Aortic Balloon Catheter Kit because of infrequent device malfunction that could lead to serious health consequences. 44,807 units are affected worldwide.
The FDA recalled 3,138 Arrow Ultra 8 intra-aortic balloon catheter kits globally due to potential balloon inflation failure and helium pathway damage that could compromise critical cardiac support.
The Arial mobile application experiences frequent restarts on iOS 17.4 and 17.5, causing alert overload, communication failures, and offline status in healthcare facilities.
Glenmark Pharmaceuticals is recalling Rizatriptan Benzoate 10mg tablets nationwide due to N-nitroso impurity levels exceeding FDA acceptable limits, affecting 13,296 cartons.
CORENTEC is recalling LOSPA Tibial Insert knee implant components due to an unsupported 10-year expiration date. Patients with these devices should consult their physician.
CORENTEC's LOSPA Patella Component knee implants are recalled due to an unsupported 10-year expiration date. Thirty-five units were distributed nationwide.
Oil may leak from the HA FlexTrak patient transport device when the hydraulic pedal is pressed, creating a potential slipping or falling hazard on the floor.
Atrium Medical Corporation recalls Advanta VXT vascular grafts due to separation of internal swivel components. Approximately 53,308 units worldwide are affected, with the slider GDS swivel rod potentially separating from its core.
Atrium Medical is recalling ADVANTA VXT vascular grafts following complaints of separation between the slider component and swivel core.
Atrium Medical Corporation is recalling ADVANTA VXT vascular grafts due to reported separation of the Slider GDS Swivel Rod from the Swivel Core. Approximately 53,308 units have been affected worldwide.
Atrium Medical Corporation is recalling ADVANTA VXT vascular grafts due to reported separation of the Slider GDS Swivel Rod from the Swivel Core. No injuries have been reported.
Atrium Medical recalls ADVANTA VXT vascular grafts due to reported separation of the slider swivel rod from its core, creating a gap between components. No injuries reported.