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.
Hospira is recalling 301,560 bags of 5% Dextrose Injection due to potential punctures that may compromise sterility and cause leaks.
Hospira is recalling 836,460 bags of Potassium Chloride IV solution due to potential punctures that may compromise sterility and cause leaks.
Philips Medical Systems is recalling Gel-E Donut and Squishon 2 baby support products because mold was found on the gel-filled items.
Marathon Ventures Inc. is recalling various brands of macadamia nuts nationwide due to possible contamination with Salmonella florida.
Hospira is recalling 823,296 bags of 5% Dextrose and 0.45% Sodium Chloride Injection due to potential punctures that may compromise sterility.
Hospira is recalling 152,172 bags of Normosol-R IV solution due to potential punctures that may compromise sterility and cause leaks.
Abbott Ireland Diagnostics Division is recalling 7,415 ARCHITECT Total T3 Reagent Kits because 17% of specific lots may produce patient results higher than expected.
Los Chileros De Nuevo Mexico is recalling Blue Corn Waffle & Pancake Mix and six other products due to undeclared wheat.
Los Chileros De Nuevo Mexico is recalling seven food products, including Carne Adovada and Sopaipilla Mix, due to undeclared wheat.
Respironics is recalling Esprit V1000 and V200 Conversion Ventilators because incorrect screw installation may cause a short circuit, preventing the switch to battery power during AC outages.
Los Chileros De Nuevo Mexico is recalling seven food products, including soups and mixes, due to undeclared wheat.
Toshiba American Medical Systems is recalling one unit of cardiac function analysis software in the US because it may display incorrect analysis results.
Hospira is recalling 16.5 million bags of 0.9% Sodium Chloride Injection due to potential punctures that may compromise sterility and cause leaks.
Hospira is recalling GemStar infusion pumps because patients are accessing dosage reset codes to change infusion rates set by doctors.
Prevost is recalling 80 model year 2009-2011 X3 and XL2 motorcoaches because the fire suppression tank may vent, rendering the system inoperable during a fire.
Gyrus Acmi is recalling Falope-Ring Band Applicator Kits due to sterile packaging compromises that could lead to bacterial contamination and patient infection.
Los Chileros De Nuevo Mexico is recalling seven food products, including cornbread and mixes, because they contain undeclared wheat.
Los Chileros De Nuevo Mexico is recalling seven food products, including Santa Fe Chile Seasoning, due to undeclared wheat.
Nova Bus is recalling 2012 LFS transit buses because a seat anchor rivnut may not secure the seat properly, increasing injury risk if the seat detaches.
Temsa is recalling 38 model year 2014-2015 TS45 motorcoaches because a headlamp control module malfunction may cause headlamps and daytime running lamps to fail while driving.
Los Chileros De Nuevo Mexico is recalling seven food products, including Green Chile Stew with Tortilla Mix, because they contain undeclared wheat.
Hospira Inc. is recalling GemStar infusion pumps because patients are using publicly available codes to change infusion rates set by doctors.
Los Chileros De Nuevo Mexico is recalling Sopaipilla Mix and other products due to undeclared wheat, posing a risk to individuals with wheat allergies or celiac disease.
Discus Dental LLC is recalling Relief ACP Oral Care Gel because some units were filled with hydrogen peroxide instead of phosphate gel, potentially causing increased sensitivity.
Materialise USA LLC is recalling specific Zimmer Patient Specific Instrument PERSONA CR Pin Guides because the packaging contained incorrect components and one guide exceeded size specifications.