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.
Orbea is recalling 715 Avant bicycles because the front fork can crack, posing a fall hazard. No injuries have been reported.
iDevices is recalling about 48,500 cooking thermometer probes in the U.S. and 510 in Canada because the internal plastic insulator can melt and fall into food.
Medtronic is recalling MiniMed Paradigm insulin pumps because users may have accidentally programmed them to deliver the maximum bolus amount.
Zimmer, Inc. is recalling 15 units of a specific knee prosthesis component because internal review found five raw material forgings with defects that were not segregated.
Thermedx LLC is recalling 21 units of the P4000 Fluid Management System because a manufacturing change to the canister ring may cause the deficit display to read higher than the actual fluid deficit.
Beta Labs is recalling Oxyphen XR fat burner capsules because they contain DMAA, a substance not permitted in dietary supplements.
Novel Laboratories is recalling 25,776 containers of Famotidine Oral Suspension because the product failed an impurity specification. The recall is classified as FDA Class III.
Mylan Pharmaceuticals is recalling Diltiazem HCl Extended Release Capsules because routine stability testing found high levels of a related compound.
Ford is recalling specific 2014 Focus, 2014 Escape, and 2015 Lincoln MKC vehicles because a fuel delivery module may crack, causing low fuel pressure and potential vehicle stalls.
Ford is recalling 2015 F-650 and F-750 SD trucks because a fuel filter defect may cause the engine to stall without warning, increasing crash risk.
Mitsubishi is recalling 2010-2014 i-MiEV electric vehicles because the brake vacuum pump may stop functioning, potentially increasing stopping distance and crash risk.
Genera is recalling specific aftermarket headlamp assemblies for 2013-2014 Acura ILX vehicles due to overheating risks that could cause smoke, melting, or fire.
Trimas is recalling specific Highland and Reese roof rack carriers because they may lack warning labels against using them with cargo bags or boxes.
Tray Vous is recalling snack and activity trays for strollers because the design poses a strangulation hazard to unharnessed children.
Gillig is recalling 231 model year 2014 Low Floor transit buses because a fuel filter defect may cause the engine to stall unexpectedly, increasing the risk of a crash.
New Flyer is recalling 2014 transit buses because a fuel filter defect may cause the engine to stall without warning, increasing the risk of a crash.
General Motors is recalling specific 2013-2014 Cadillac XTS and Chevrolet Impala vehicles because the air bag control module may be in manufacturing mode, preventing deployment in a crash.
American Woodcrafters is recalling about 1,900 Cottage Retreat II bunk beds sold at Havertys because side support rails can break, posing a fall hazard.
Baxter Healthcare is recalling 4,200 containers of 0.9% Sodium Chloride Injection because blue polyisoprene shavings were found inside the bag port tubes.
Natural Grocers by Vitamin Cottage is recalling Chunks of Energy products due to the potential presence of Salmonella.
Ben Venue Laboratories is recalling 7,172 vials of Cytarabine for Injection due to potential crimp defects that may affect sterility.
AngioDynamics is recalling Uni*Fuse Infusion Systems with Cooper Wire because they may contain a guidewire that is too long.
Ortho Development is recalling specific knee implant components because defective foil pouches allowed air to enter, potentially degrading the material properties of the implants.
Childrens Medical Ventures is recalling Gel-E Donut and Squishon 2 gel pillows because of visible mold. The mold was identified as Cladosporium and Penicillium fungi.
Goodman Company is recalling approximately 233,500 packaged terminal air conditioners and heat pumps because power cords can overheat, posing fire and burn risks.