State
73,824 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 73,824 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
Hospira is recalling 181,704 bags of Magnesium Sulfate in Dextrose because some units may have incorrect barcodes that scan as heparin sodium.
Janssen Pharmaceuticals is recalling Ortho-Cept tablets because they contain less active ingredient than labeled. The recall covers 16,861 cartons distributed in the US and Canada.
Honda is recalling 2014-2015 Acura MDX, RLX, and RLX Hybrid vehicles because the Collision Mitigation Braking System may unexpectedly apply brakes, increasing crash risk.
HeartWare Inc is recalling HVAD Pump Driveline Splice Kits because they may fail if exposed to excessive force. The recall affects 35 units distributed in the US and several international countries.
Starcraft is recalling 2006-2015 transit buses because a loose electrical connection may cause overheating and fire.
Valor Athletics is recalling 100 Olympic weight benches because a weld can break, posing an injury risk. No injuries have been reported.
Gourmet Kitchen, Inc. is recalling 394 boxes of Spicy Shrimp Chopsticks because the products may contain peanut protein.
Hewitt is recalling about 1,700 chain-driven marine winches because the roller chains can break, posing an injury risk to users and bystanders.
Gourmet Kitchen, Inc. is recalling Lobster Spring Rolls because they may contain peanut protein. The recall covers 42 boxes distributed nationwide.
Philips Medical Systems is recalling 918 ADAC Vertex Gamma Cameras because detector heads may drift and contact patients during imaging.
Forest River is recalling 2014-2016 Vengeance trailers because incorrect certification labels may cause operators to overload the vehicle, increasing crash risk.
Gourmet Kitchen, Inc. is recalling Shrimp Maui products because they may contain peanut protein. The recall covers 135 boxes distributed nationwide.
Gourmet Kitchen, Inc. is recalling Asparagus Roll Ups because the products may contain peanut protein. The recall covers 315 cases distributed nationwide.
Gourmet Kitchen, Inc. is recalling Spinach & Goat Cheese Focaccia because the product may contain peanut protein, posing a risk to individuals with peanut allergies.
Electrolux is recalling Kenmore Elite slide-in ranges sold at Sears because a sharp edge on the stainless steel trim below the control panel can cause cuts.
Electrolux is recalling about 250 Kenmore Elite dual fuel ranges sold at Sears because the burner flame can go out while gas is on, posing fire and burn risks.
Gourmet Kitchen, Inc. is recalling Lobster & Shrimp Spring Rolls because they may contain peanut protein. The recall covers 120 boxes distributed nationwide.
Natural Foodworks Group is recalling Purely Elizabeth Cranberry Cashew Ancient Grain Muesli because it contains undeclared sulfur dioxide.
Alvogen, Inc. is recalling Nitrofurantoin Monohydrate/Macrocrystalline capsules because they failed a dissolution specification test.
Akorn, Inc. is recalling specific lots of Sulfamethoxazole and Trimethoprim Oral Suspension because the sulfamethoxazole failed to meet dissolution specifications.
Synthes, Inc. is recalling 8,175 TFNA Proximal Femoral Nails because the locking mechanism was assembled too close to the top, potentially causing surgical delays.
Akorn, Inc. is recalling specific lots of Sulfamethoxazole and Trimethoprim Oral Suspension because the sulfamethoxazole component failed to meet dissolution specifications.
BioHorizons is recalling 48 units of the Tapered HD Upgrade Set because they were packaged with a stainless steel drill instead of the correct titanium component.
Apotex Inc. is voluntarily recalling 6,467 units of Olanzapine 10 mg orally disintegrating tablets because the drug is subpotent.
Philips Medical Systems is recalling 975 nuclear gamma cameras because the collimator exchange carriage and storage cabinet were misaligned.