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.
Louis Garneau is recalling about 1,180 P-09 aerodynamic bicycle helmets because they may fail to protect the wearer from impact injuries in cold temperatures.
Fluid Handling is recalling McDonnell & Miller low water cut-off control units for hot water or steam boilers due to fire and explosion hazards.
General Motors is recalling 2015 Chevrolet Colorado and GMC Canyon vehicles because incorrect driver air bag wiring may disrupt deployment timing, increasing injury risk in crashes.
Rejuvenation is recalling about 85 Haleigh Wire Dome Pendant lamps because the cord system can fail, causing the lamp to fall and pose a risk of injury.
Baxter Healthcare is recalling 50,530 bags of Dianeal Low Calcium peritoneal dialysis solution due to the presence of particulate matter found during manufacturing.
Chrysler is recalling 2014 Ram ProMaster vehicles because the tire pressure monitoring system may fail to detect low tire pressure, increasing crash risk.
The FDA is recalling CUBICIN daptomycin injection vials because there may be glass particles present in the vials.
Chrysler is recalling 2011-2013 Jeep Wranglers because corrosion in the heated mirror connector may cause an electrical short and fire.
PAB Two is recalling ThermalStrike Expedition bed bug heat treatment systems because a flexible electrical strip can break, posing a fire hazard.
Sagent Pharmaceuticals is recalling 10,622 bags of Zoledronic Acid Injection because of a lack of assurance of sterility and leaking premix bags.
Chrysler is recalling 2014 Jeep Grand Cherokee and Dodge Durango vehicles because a software issue may disable Electronic Stability Control, increasing crash risk.
Continental is recalling specific ProContact GX SSR MOE tires used on 2015 Mercedes-Benz C-Class vehicles due to potential deformation during curing that could cause sudden tire failure.
Baxter Healthcare is recalling 11,808 bags of Dopamine Hydrochloride and Dextrose due to a potential manufacturing defect that may compromise sterility.
Buddy's Kitchen is recalling approximately 62,488 pounds of meat and poultry breakfast products due to possible Listeria monocytogenes contamination. No illnesses have been reported.
Hospira is recalling 40,730 vials of Marcaine (bupivacaine hydrochloride) injection because of a confirmed complaint of visible metal particles in the solution.
Fiskars is recalling 32-inch bypass lopper shears sold at Home Depot because the handles can break, posing a risk of serious injury and laceration.
Chrysler is recalling 2010-2014 Ram trucks because diesel fuel heater connectors may overheat, potentially causing fuel leaks and fire.
AbbVie is recalling 18,021 bottles of CREON (pancrelipase) capsules because some bottles contain foreign tablets or co-mingled LipaCreon 13000.
Teleflex Medical is recalling Hudson RCI Pediatric Anesthesia Breathing Circuits because they can crack prior to and during use.
Chrysler Group is recalling specific 2011-2014 models because the alternator may fail, causing the vehicle to stall without warning and increasing crash risk.
Siemens is recalling Ysio Max radiographic systems because a malfunction can cause images to be lost, requiring patients to repeat examinations.
Siemens is recalling AXIOM Luminos dRF Max systems due to malfunctions that cause lost images and incorrect labels, potentially leading to repeated examinations.
Siemens is recalling two Uroskop Omnia Max systems because a malfunction causes image loss and incorrect labels, leading to repeated examinations.
Siemens is recalling five Luminos Agile Max systems due to malfunctions that cause image loss and incorrect labels, leading to repeated examinations.
Zimmer, Inc. is recalling 16,380 units of Persona The Personalized Knee System 2.5 mm Female Screws due to potential stripping of the hex driver when used in cortical bone.