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.
Lupin Pharmaceuticals is recalling 111,648 bottles of Duloxetine 30 mg capsules because they failed to meet dissolution standards.
Siemens Healthcare Diagnostics is recalling Dimension Vista Protein 1 Control H due to inaccurate ceruloplasmin test results.
Arrow International is recalling VPS Access Kits because they may contain 5 Fr peel-away sheaths instead of the required 4 Fr size.
Implant Direct Sybron Manufacturing is recalling 75 units of Legacy 3 Dental Implants because a packaging defect may compromise sterilization.
Arrow International is recalling specific lots of ARROW PICC powered by ARROW VPS Stylet kits that may contain 5 Fr peel-away sheaths instead of the required 4 Fr.
Mayne Pharma Inc is recalling 11,364 bottles of Liothyronine Sodium Tablets 25 mcg because they failed dissolution specifications. The affected lot is distributed nationwide.
Medtronic is recalling 21 units of Everflex Self-Expanding Peripheral Stents because the stent length on the label may not match the actual stent length.
Netgear is recalling VMA4700 power adapters for Arlo outdoor cameras because water leakage can cause short circuits, melting, and fire.
Metabo is recalling specific rat tail angle grinders because the on-off switch can lock in the on position, posing a laceration hazard.
Burch Tank and Truck is recalling 1984 Evans Cargo Tank trailers because improperly torqued brake caliper bolts may allow the caliper to detach, increasing crash risk.
Triple E RV is recalling 2016-2018 Wonder motorhomes because improperly tightened passenger seat bolts may fail in a crash, increasing injury risk.
West Elm is recalling about 43,000 Industrial Task table lamps because the electrical wire can be cut or frayed, posing a risk of electric shock.
Temsa is recalling 2017-2018 TS30, TS35E, and TS45 buses because the fire suppression system may contain contaminated dry chemical, which could discharge improperly and increase injury risk.
Ford is recalling 2018 Expedition vehicles because second-row outboard seats may have improperly installed bolts or excessive forward adjustment, increasing injury risk in a crash.
MV Agusta is recalling 45 2017 Brutale 800 Dragster RR motorcycles because rear wheel spokes may loosen, potentially affecting handling and increasing crash risk.
Camso is recalling DTS 129 conversion kits because a brake pin can loosen, posing a crash or impact hazard. No injuries have been reported.
Kia is recalling 2012-2014 Forte and Forte Koup vehicles because a deteriorating brake pedal stopper pad may keep brake lights on or allow shifting without pressing the brake pedal.
Kawasaki is recalling 2017-2018 Z125 PRO motorcycles because an ECU software defect may cause the engine to stall, increasing crash risk.
Hyundai is recalling 2013-2014 Elantra vehicles because a deteriorating brake pedal stopper pad can cause brake lights to stay on and allow shifting out of park without pressing the brake pedal.
Natural Solutions for Life is recalling Synodrin Pain Relieving Cream because the jar caps are not child-resistant, posing a poisoning risk to young children.
Flos Inc. is recalling specific Romeo Moon and Romeo Louis II pendant light fixtures because the internal glass diffuser can detach and fall, posing an impact injury hazard.
Kubota is recalling approximately 26,900 RTV-X series utility vehicles because seat belt stays can break, posing an injury hazard in a crash.
Zimmer Biomet is recalling 18 units of ROSA Brain 3.0.0 software due to communication errors between software components and the controller.
Spacelabs Healthcare is recalling 110 Arkon Anesthesia Workstations due to failures in ventilation, gas delivery, and display alarms.
Bugatti is recalling 2017-2018 Chiron vehicles because front seat recliner brackets may not be welded properly, which could cause the seat to move unexpectedly and increase crash risk.