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.
WhiteWave Foods is recalling Horizon Cheddar Sandwich Crackers because they may contain undeclared peanuts due to a packaging error.
Brinkhoff & Monoson Inc is recalling HT Traders Blue Cheese Jalapeno Spicy & Unique Seasoning Blend because it may contain undeclared peanut allergens.
Baxter Healthcare is recalling 196,128 containers of 0.9% Sodium Chloride Injection due to lack of sterility assurance and leak complaints.
Baxter Healthcare is recalling 7,444 containers of Clinimix E 5/20 due to a lack of assurance of sterility and increased leak complaints.
Pega Medical Inc. is recalling 7 units of the 4.8mm GAP Nail because of failures at the distal cortical screw holes, primarily in patients with specific bone conditions.
Medtronic is recalling 6,040 Model 5392 temporary pacemakers because specific AA batteries may fail to connect, potentially stopping pacing therapy.
Maternal Science Inc. is recalling Healthy Mama Boost It Up Mighty Mango Protein Drink because it contains undeclared milk.
Zenobia Company LLC is recalling My Spice Sage Ground Cumin because it may contain undeclared peanut protein. The recall covers 1,467 units sold nationwide.
Maternal Science Inc. is recalling Healthy Mama Boost It Up Mango with Ginger Protein Drink because it contains undeclared milk.
KTM is recalling 409 model year 2015 690 Enduro R motorcycles because the rear brake line may be damaged, potentially causing a loss of braking ability and increasing crash risk.
Brinkhoff & Monoson Inc is recalling Archer Farms ground cumin because it may contain undeclared peanut allergens.
Brinkhoff & Monoson is recalling Dark Chili Powder distributed by The Fresh Market because it contains cumin that may be contaminated with undeclared peanut allergens.
Gilster-Mary Lee Corp. is recalling Honey & Oat Mixers dry cereal because it contains undeclared almonds, a major food allergen.
DePuy Orthopaedics is recalling 54 units of the RECLAIM Assembled Implant Inserter Adaptor because the instrument may fracture during surgery, potentially leaving plastic pieces in the patient.
Maternal Science Inc. is recalling 60 units of Healthy Mama Boost it Up Pom Cherry Caffeine Free Protein with Energy Drink because it contains undeclared milk.
See's Candies is recalling 8 oz. Classic Red Hearts with Assorted Chocolates because the packaging failed to list tree nuts in the ingredient statement.
Biomet, Inc. is recalling 50 units of Ziploop Buttons and ToggleLocs manufactured in 2014 because sterile packaging was not properly sealed.
Michael Foods is recalling 181,127 cases of frozen egg patties because they contain milk, an allergen not declared on the label.
Microtek Medical Inc. is recalling 270 units of sterile laparoscopic tubing sets because the packaging contains latex but lacks the required warning label.
Edwards Lifesciences is recalling specific sizes of the Fem-Flex II Pediatric Femoral Arterial Cannula due to a protruding wire at the tip that could cause tissue damage.
Dimension Industries is recalling Hampton Bay-branded patio set rockers sold at Home Depot because the chairs can break during normal use, posing a fall hazard.
Microtek Medical Inc is recalling 38 units of FREEDOMAIRE Motor Modules because the packaging contains latex but lacks the required warning label.
Microtek Medical is recalling smoke evacuator tubing sets because the packaging contains latex but lacks the required warning label.
Smooth Industries is recalling about 7,600 children's pajamas that fail federal flammability standards, posing a risk of burn injuries.
Biomet is recalling ToggleLoc and Ziploop devices manufactured in 2014 because sterile packaging was not sealed, potentially compromising sterility.