State
73,827 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 73,827 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
Tishomingo is recalling 2012-2015 Quarter Frame dump trailers because the draft arm may crack or break, potentially causing loss of vehicle control.
Ameritrans is recalling 2013-2014 F330 and 2013 R330 transit buses because a suspension fluid tank mount may fail, causing the tank to separate and create a road hazard.
Aircraft Medical Limited is recalling McGrath MAC2 Video Laryngoscope Blades because the retaining clip may be difficult to engage, increasing the risk of the blade disconnecting during intubation.
Teleflex Medical is recalling Aquapak Nebulizer Adaptors because packaging seals may be open or weak, potentially compromising the sterility of the devices.
Gambro Renal Products Inc is recalling Polyflux Revaclear and Max Dialyzers because potential tears in the packaging may compromise the sterile barrier.
Amerx Health Care Corp. is recalling Amerigel Hydrogel Wound Dressing units due to a formulation deviation. The recall covers 340,896 units distributed nationwide and internationally.
Teleflex Medical is recalling Aquapak nebulizer adaptors because packaging seals may be open or weak, potentially affecting the sterility of the device.
GCI Outdoor is recalling about 6,000 BleacherBack stadium seats because the backrest can fail, posing a risk of injury. Consumers should stop using the seats and contact the company for a repair kit.
Gambro Renal Products Inc is recalling Polyflux Revaclear and Max Dialyzers because potential tears in the packaging may compromise the sterile barrier.
Alcon is recalling INFINITI Vision System Ultrasound FMS units because pieces of tubing may be present in the aspiration line.
Cure Medical is recalling pediatric urinary catheters because some boxes are mislabeled as size 8 but contain size 10 catheters, posing a risk of injury.
Ethan Allen is recalling Harwood floor lamps because a defect in the line cord insulation poses a risk of electrical shock. One incident of electrical shock has been reported.
Ethicon is recalling PERMA-HAND silk sutures because the company cannot ensure the products meet the expected sterility assurance level.
Integra LifeSciences is recalling 6,358 Selector Kit tubing units because they may leak irrigation fluid during use if not placed correctly on the handpiece.
Siemens is recalling 1,131 Artis zee and zeego Angiography Systems due to a software issue that prevents deactivating the radiation block function after a network problem.
Beevers Manufacturing recalled 393 units of Cannulaide Model 101 because the product was packed and labeled as Model 102.
Amerx Health Care Corp. is recalling 1,740 units of Amerigel Daily Dressing Packets due to a formulation deviation. The affected products were distributed nationwide and internationally.
Amerx Health Care Corp. is recalling 79,677 Amerigel Post-op Surgical Kits due to a formulation deviation. The affected kits were distributed nationwide and internationally.
Sandoz, Inc. is recalling 6,336 bottles of 16 mg candesartan cilexetil tablets because stability testing showed impurity levels exceeded specifications.
Amerx Health Care Corp. is recalling 21,108 units of Amerigel Saturated Gauze Dressing due to a formulation deviation. The products were distributed nationwide and internationally.
Microgenics Corporation is recalling 2,135 vials of MAS CardioImmune XL Cardiac Marker Control (Lot CXL16011) because the product shows vial-to-vial variation for specific analytes.
Zydus Pharmaceuticals USA is recalling Benzonatate 200 mg capsules because they may contain foreign 100 mg capsules.
Hyundai is recalling specific 2015 Sonata vehicles because an incorrect left axle shaft may separate from the transaxle, potentially causing the vehicle to stop moving or roll away.
Cummins is recalling specific Ecofit Tier2 DOC raincaps because the lid may detach, posing a crash or injury risk.
Lenovo is recalling LS-15 AC power cords for laptops due to overheating risks that can cause fires and burns. Consumers should stop using the cords and contact Lenovo for a free replacement.