State
73,817 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 73,817 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
Bugatti is recalling 2006-2008 Veyron vehicles because corrosion on the battery cable may cause overheating and increase the risk of a fire.
Soaring Helmet Corporation is recalling Vega CFS helmets that may not adequately protect users in a crash, failing to meet federal safety standards.
Bugatti is recalling 2006-2011 Veyron and Veyron Grand Sport vehicles because the fuel gauge may display more fuel than is actually in the tank, increasing the risk of stalling and a crash.
Soaring Helmet Corporation is recalling Stealth Phantom helmets that may not adequately protect wearers from penetration injuries in a crash.
Nissan is recalling 2016 Maxima and Murano vehicles because a damaged O-ring in the ABS actuator may reduce brake fluid pressure, increasing crash risk.
Toyota is recalling 2016 RAV4, Lexus RX350, and ES350 vehicles because a damaged O-ring in the ABS actuator may cause improper brake fluid pressure control, increasing crash risk.
Deca International is recalling GolfBuddy BB5 GPS bands because charging ports can produce an electrical charge that burns exposed skin. Two consumer burn reports have been received.
Cruiser RV is recalling 2016-2017 Stryker travel trailers because the safety chains are rated for less weight than the trailer's gross vehicle weight rating.
Rainbow Play Systems is reannouncing a recall of plastic yellow trapeze rings that can crack or break, posing a fall hazard to children.
Toyota is recalling 2016 Sienna minivans because incorrect front seat belt height adjusters may tear or separate during a crash, increasing injury risk.
Jayco is recalling 43 model year 2016 Octane travel trailers because crossed turn signal wires may activate the wrong light, increasing crash risk.
Soaring Helmet Corporation is recalling Vega XTV 7400 helmets that may not adequately protect users in a crash. Owners can exchange the helmets or receive a refund.
IKEA is recalling children's LATTJO bat cape costumes because the neck fastener can fail to detach, posing a strangulation hazard.
ProSupps USA LLC is recalling Mr. Hyde Intense Energy Pre-Workout supplements because they may contain the undeclared non-dietary ingredient Picamilon.
ProSupps is recalling Dr. Jekyll Intense Pump Pre Workout due to potential mislabeling and the presence of the non-dietary ingredient Picamilon.
Dr. Reddy's Laboratories is recalling 3,342 vials of Zoledronic Acid Injection due to defective seals that may compromise sterility.
Siemens is recalling 124 SOMATOM Emotion and Sensation CT systems due to a potential malfunction in cardio licenses that could hazard patients and personnel.
Advics is recalling ABS brake actuators for Toyota and Nissan vehicles due to a damaged O-ring that may cause a lack of brake fluid pressure.
Tesla is recalling 2,676 Model X vehicles because the third row seat back may move forward in a crash, increasing injury risk.
Nipoamerican is recalling specific Elegance and Evolution mattresses because they fail to meet federal open flame standards. Consumers should contact the company for free protective covers.
Siemens is recalling 124 SOMATOM Emotion and Sensation CT systems due to a potential malfunction hazard when using specific cardio licenses.
Siemens is recalling 552 Artis zeego angiography systems due to risks of mechanical cable damage and high-voltage generator module failure.
Mitsubishi Heavy Industries is recalling VERO MHI-TM2000 Linear Accelerators because the operator console may set an incorrect gantry angle for the first beam of an IMRT treatment.
Terumo is recalling 222 CDI Blood Parameter Monitoring System 500 devices because a faulty thermistor may cause inaccurate temperature and analyte readings.
Roche Diagnostics is recalling the Elecsys Estradiol II assay because fulvestrant treatment causes falsely elevated estradiol results.