State
73,741 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 73,741 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
E-One is recalling 2001-2002 X-036 and X-113 emergency vehicles because fire pump manifold end caps may fail, causing sudden water discharge or pressure loss.
E-One is recalling 2013-2017 Quest II, Cyclone II, and Typhoon emergency vehicles because a missing diode may damage the starter lock-out relay, preventing the vehicle from starting.
Skip Hop is recalling Tuo convertible high chairs because the front legs can detach, posing a fall hazard to children.
Jaguar Land Rover is recalling 2009-2010 Range Rovers because the passenger air bag inflator may explode during deployment, potentially causing serious injury or death.
Jaguar Land Rover is recalling 2010-2012 Range Rovers because passenger air bag inflators may explode during deployment, posing a risk of serious injury or death.
Jaguar is recalling 2010-2015 XF vehicles because the front passenger air bag inflator may explode during deployment, potentially causing serious injury or death.
Jaguar is recalling 2009-2013 XF vehicles because the front passenger air bag inflators may explode during a crash, potentially causing serious injury or death.
Terex is recalling 2015-2017 XT Pro 56 and 60 aerial devices because the platform control enable system may be adjusted incorrectly, increasing injury risk.
McLaren is recalling 371 2013 MP4-12C vehicles because the passenger air bag inflators may explode during deployment, posing a risk of serious injury or death.
Crescent City Meats is recalling approximately 430 pounds of ready-to-eat Tasso Cajun Spicy Ham because the product may be underprocessed and undercooked.
HP is recalling about 50,000 lithium-ion batteries for notebook computers and mobile workstations because they can overheat, posing fire and burn hazards.
Volkswagen Group of America is recalling specific Audi models because passenger air bag inflators may explode during deployment, posing a risk of serious injury or death.
Gulf Stream is recalling 2011-2012 recreational trailers because the installed fire extinguishers may clog or detach, potentially failing to discharge or causing injury.
Altec Industries is recalling 2010-2011 Effer 440 and 470 Knuckle Boom Cranes because rotation bearing fasteners may fail, causing the pedestal to crack and increasing injury risk.
SureFit is recalling about 900 riding lawn mower blade spindle shafts and assemblies because they can break and become projectiles, posing an impact injury risk.
Sterilmed Inc is recalling 112 reprocessed St. Jude Medical Agilis NxT Steerable Introducers due to inadequate seals caused by missing adhesive glue.
Forest River is recalling 2018 Glaval Legacy buses because improperly tightened brake caliper bolts may cause the calipers to detach, reducing braking power and increasing crash risk.
L3 Security & Detection is recalling 471 Examiner 3DX 6000 cabinet X-ray systems used for airline baggage screening due to shielding gaps that may cause excessive X-ray emissions.
Philips is recalling specific IntelliVue patient monitors and measurement servers because they may display distorted ST-segments during 12-lead ECG monitoring.
Medline Industries is recalling 5,722 units of sterile elastic bandages because they may not have been properly sterilized.
Remel Inc is recalling Shigella sonnei Agglutinating Serum because it may fail to agglutinate within the specified minimum reaction time.
Pharmedium Services LLC is recalling morphine sulfate injection due to incorrect or missing lot and expiration dates on the labels.
Pharmedium Services LLC is recalling Hydromorphone HCl Injection due to incorrect or missing lot and expiration dates.
Pharmedium Services LLC is recalling specific lots of compounded morphine sulfate injection because the labels may have incorrect or missing lot and expiration dates.
Keryx Biopharmaceuticals is recalling Auryxia (ferric citrate) tablets because damaged silica gel packets may allow desiccant granules to contact the medication.