State
73,817 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 73,817 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
Black Diamond is recalling Index Ascenders because a rivet may release, causing the device to detach from the rope and posing a risk of injury or death.
Rocky Mountain is recalling bicycles with front disc brakes because the quick-release lever may contact the brake rotor, causing a crash. No injuries have been reported.
Black Diamond is recalling approximately 45,500 Camalot and Camalot Ultralight climbing devices because they can come apart during use, posing a fall hazard.
Garden of Life is recalling Raw Meal Organic Vanilla Powder products due to possible Salmonella contamination. The recall covers multiple lot codes distributed nationwide and internationally.
Garden of Life is recalling Raw Meal Organic Chocolate Powder products due to possible Salmonella contamination. The recall covers 422,923 units distributed nationwide and internationally.
Garden of Life is recalling Raw Meal Organic Original Powder products due to possible Salmonella contamination. The recall affects 422,923 units distributed nationwide and internationally.
Garden of Life is recalling Raw Meal Organic Vanilla Spiced Chai Powder due to possible Salmonella contamination. The product was distributed nationwide and in several international markets.
Health 4 Life, LLC is recalling Passion 4 Life bottles because they contain undeclared whey protein and soy lecithin, posing a risk to people with allergies.
Bradshaw Medical Inc. is recalling 3,760 Axial Torque Limiting Drivers because a component failure could cause applied torque to exceed the calibrated setting.
St. Jude Medical is recalling 127 Ellipse ICD devices because they may fail to deliver high-voltage therapy needed to treat life-threatening heart rhythms.
Stoughton is recalling 324 model-year 2014 trailers because suspension pivot bolts may fail, potentially causing the axle to separate from the trailer.
Autocar is recalling 67 Xpeditor vehicles because improperly bent tab lock washers may allow rear axle spindle nuts to loosen, increasing crash risk.
Stryker is recalling CinchLock SS Knotless Anchors after reports of internal wire breakage upon deployment.
Autocar is recalling 43 model year 2016-2017 Xpert and Xspotter trucks because improperly bent tab lock washers may allow rear axle spindle nuts to loosen, potentially causing the wheel assembly to separate.
Atlas Spine, Inc. is recalling 16 Torque Limiting Handles because they were not appropriately set to mitigate the risk of implant fracture during rotation.
Siemens Healthcare Diagnostics is recalling Dimension Vista Uric Acid assays because NAC and Metamizole can cause falsely depressed results.
Medtronic is voluntarily recalling battery packs for the Capnostream 20 and 20p patient monitors because they may experience thermal runaway, posing a potential fire risk.
Heartland is recalling 2016-2017 Fair Field, Lakeview, and Resort trailers because safety chains may break if the main connection fails, increasing crash risk.
Stryker is recalling CinchLock Knotless Anchors after 13 reports of internal wire breakage upon deployment.
CVS Health is recalling Gold Emblem Abound Organic Spiced Herbal Tea because the product contains Salmonella. Consumers should stop using the product.
Lakota is recalling 2014 Luxe trailers because the built-in microwave may start on its own, posing a fire hazard.
Novarad Corporation is recalling specific versions of NovaPACS Diagnostic Viewer because the PET/CT fusion tool calculates incorrect SUV values.
Covidien LLC is recalling Bravo pH capsule delivery devices due to a potential risk of allergic reactions in patients with nickel sensitivity.
phil&teds is recalling about 630 Dash v5 strollers in the U.S. because the folding hinge can become damaged, posing a pinch hazard to consumers.
FDA is recalling the Given Imaging Bravo pH capsule delivery device due to a potential allergic reaction risk for patients with nickel sensitivity.