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.
West Elm is recalling Jensen rectangular glass tables because the tempered glass tops can shatter unexpectedly, posing a laceration hazard.
Tea Collection is recalling about 3,800 children's rompers because snaps near the collar can detach, posing a choking hazard to young children.
Gulf Stream is recalling 2018 Matrix and Geo recreational trailers because the Federal Certification Labels incorrectly list the rear axle weight rating.
Ford is recalling 2018 Escape and Lincoln MKC vehicles because incorrect front brake hoses may chafe and leak fluid, increasing stopping distance.
Mitsubishi is recalling 2011-2016 Outlander Sport vehicles because water intrusion may corrode the wiper link, causing wipers to stop working and reducing visibility.
Volkswagen is recalling 2017-2018 Tiguan Limited vehicles because the front driver air bag may not be intended for US use, failing federal safety standards and increasing injury risk in a crash.
Fujitsu is recalling specific lithium-ion battery packs for notebook computers and workstations because they can overheat, posing fire and burn risks.
Micro Bird is recalling 2015-2018 T-Series transit buses because seat belt attachments may not remain secured to the floor in a crash, increasing injury risk.
Poppin is recalling about 2,800 Pitch rolling chairs because the seat plate can break and detach, posing a fall hazard. No injuries have been reported.
Chrysler is recalling 2017 Jeep Wrangler and Dodge Caravan vehicles because brake switches may malfunction, allowing the vehicle to shift out of Park without the brake pedal being pressed.
BMW is recalling 2018 Rolls-Royce Ghost vehicles because head air bags may not fully inflate during a crash, increasing injury risk.
Halcore Group is recalling 2017 AEV Traumahawk ambulances because a battery isolator module may overheat, posing a fire and injury risk.
Husqvarna is recalling about 7,100 residential zero turn riding mowers because a fuel line defect can cause leaks and fire. No injuries have been reported.
Chrysler is recalling 2017-2018 RAM trucks because the brake pedal interlock may fail, allowing the vehicle to shift out of Park without the brake pedal being pressed.
Blue Fusion Natural is recalling Blue Pearl capsules because FDA analysis found undeclared sildenafil, an unapproved drug for erectile dysfunction.
International Laboratories, LLC is recalling Clopidogrel Tablets 75 mg because bottles were found containing Simvastatin Tablets 10 mg.
Medline is recalling Incision and Drainage Tray Kits because the Povidone-Iodine prep pads contain less iodine than labeled.
Medline Industries is recalling 60 cases of Anesthesia Kits because the Povidone-Iodine prep pads contain less iodine than the label claims.
Medline Industries is recalling Suture Removal Kits because the iodine concentration is below the label claim.
Medline Industries is recalling IV Start Kits because the iodine concentration in the prep pads is below the labeled claim.
Medline Industries is recalling sterile incision and drainage tray kits because the povidone-iodine prep pads contain less iodine than labeled.
Medline Industries is recalling 80 cases of Wound Closure Trays because the iodine concentration in the prep pads is below the labeled claim of 0.85%.
Medline Industries is recalling IV Start Kits because the iodine concentration in the prep pads is below the labeled claim of 0.85%.
Medline Industries is recalling I&D Tray Kits because the Povidone-Iodine prep pads contain less iodine than the label claims.
Medline Industries is recalling sterile Povidone-Iodine prep pads because the iodine content is below the labeled 0.85% claim.