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.
Mars Food US is recalling Uncle Ben's Ready Rice Beef Flavor pouches due to the potential for containing metal fragments.
Ameda, Inc. is recalling 1,763 units of the One-Hand Manual Breast Pump (SKU 17161) because the devices were not sterilized.
Mars Food US is recalling Uncle Ben's Ready Rice Butter & Garlic pouches due to the potential for containing metal fragments.
GE Healthcare is recalling 9,369 MRI systems worldwide because software versions were not maintained properly at some sites.
Intuitive Surgical is recalling 167 da Vinci Xi Surgical Systems worldwide because a fault causes distal SUJ failures and position sensor mismatches.
Aloha is recalling its Chocolate Premium Protein powder due to the presence of Staphylococcus enterotoxin. The product was sold nationwide online and in New York retail stores.
Mars Food US is recalling Uncle Ben's Ready Rice Original due to the potential presence of metal fragments.
FGF Brands, Inc. is recalling 7,783 cases of Mini Naan because the packages were shipped without labels declaring ingredients, nutrition, or allergens.
Intuitive Surgical is recalling 167 da Vinci Xi Surgical Systems worldwide due to a fault causing distal sensor failures and position mismatches.
Mars Food US is recalling Uncle Ben's Ready Rice Roasted Chicken Flavored with Carrots and Herbs due to the potential for containing metal fragments.
Buy4easy is recalling TMS HY-809 motorcycle half-helmets because they may fail to adequately dampen impacts and lack required labeling, increasing injury risk in crashes.
Sunfood is recalling Organic Sacha Inchi Powder because it may be contaminated with Staphylococcus enterotoxin. The product was distributed nationwide and internationally.
The Hain Celestial Group is recalling Taj Ethnic Gourmet Calcutta Masala Simmer Sauce because cumin in the product may contain undeclared peanut protein.
Stokke is recalling about 400 Trailz strollers sold in late 2014 because the handle can break, posing a fall hazard to infants. No injuries have been reported.
RaySearch Laboratories is recalling RayStation Radiation Therapy Treatment Planning System software due to an issue with photon dose calculation for Dynamic MLC plans.
Penner Mfg Inc is recalling 158 Patient Stretcher/Transfer Lift Systems because improper patient positioning could cause the device to tip, risking injury to patients or operators.
Ameda is recalling its Dual Short Term HygieniKit Milk Collections System because the devices were not sterilized. Consumers should stop using the product and contact the manufacturer.
Intuitive Surgical is recalling 167 da Vinci Xi Surgical Systems worldwide due to a fault causing distal SUJ failures and position sensor mismatches.
Siemens Medical Solutions is recalling 132 MAGNETOM MRI systems because a defect in gradient output supervision could allow outputs to exceed safety limits, potentially causing peripheral nerve stimulation.
Mars Food US is recalling Uncle Ben's Ready Rice New Orleans Style Red Beans & Rice due to the potential for containing metal fragments.
The Hain Celestial Group is recalling Taj Ethnic Gourmet Punjabi Saag Spinach Sauce because it may contain undeclared peanut protein.
CareFusion 303, Inc. is recalling 56,015 Alaris PC infusion pumps because a keypad issue may trigger an error code during the power-on self-test.
Synthes, Inc. is recalling 249 Electric Pen Drive systems because the Hand Switch labels for 'on' and 'lock' were interchanged.
West-Ward Pharmaceutical is recalling Fentanyl Citrate injections because the product failed impurity and degradation specifications and 12-month stability testing.
ArthroCare Medical Corporation is recalling 15 Coblator II systems because specific components were reversed on the controller boards.