State
73,806 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 73,806 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
Roxane Laboratories is recalling 6,493 bottles of Furosemide 20 mg tablets because a complaint reported an unusually thick tablet.
Mylan LLC is recalling specific lots of Temozolomide Capsules, 100 mg, because customer complaints reported broken or crushed capsules resulting in loose powder in the bottles.
PerkinElmer is recalling AutoDELFIA Plate Processors with Version 3.0 software due to potential plate loading failures that could affect clinical assay results.
Mylan LLC is recalling Temozolomide Capsules, 180 mg, due to customer complaints of broken or crushed capsules resulting in loose powder in the bottles.
Atrium Medical is recalling Oasis Blood Recovery Drains because the outer packaging is not sterile. The recall covers units with expiration dates prior to October 2019.
Atrium Medical is recalling 400 Series Express Drains because the outer packaging is not sterile. The recall affects approximately 1.4 million cases distributed worldwide.
Sun Pharmaceutical Industries is recalling 11,618 bottles of buPROPion Hydrochloride Extended-release Tablets due to failed dissolution specifications and stability issues.
Mylan LLC is recalling Temozolomide Capsules, 140 mg, due to customer complaints of broken or crushed capsules resulting in loose powder in the bottles.
Atrium Medical is recalling Oasis Pediatric Drains because the outer packaging is not sterile. The recall covers 964,463 US cases and 521,975 international cases.
Atrium Medical is recalling Express Mini 500 dry seal drains because the outer packaging is not sterile.
PerkinElmer is recalling AutoDELFIA systems with V3.0 software due to potential plate loading failures that could affect clinical assay results.
Roxane Laboratories is recalling 74,108 bottles of Azelastine Hydrochloride Nasal Spray because the delivery system failed droplet size testing.
PerkinElmer is recalling AutoDELFIA systems with Version 3.0 software due to potential plate loading failures that could affect clinical assay results.
Vintage Pharmaceuticals is recalling 2,568 bottles of Dexamethasone Elixir because the product failed impurity and degradation specifications.
Pentax of America is revising the Instructions for Use for Rigid Laryngostroboscopes Models 9106 and 9108.
Actavis Inc is recalling specific lots of Albuterol Sulfate Inhalation Solution because the product failed impurity specifications for a known degradant.
Simpli Home is recalling about 240 chests of drawers because they can tip over and injure children if not anchored to the wall.
3i Corporation is recalling bar chairs sold at Lowe's because legs can detach from the center post, posing a fall hazard.
Bolton Furniture is recalling approximately 1,000 4-drawer dressers because they pose a serious tip-over and entrapment hazard to children if not anchored to the wall.
Brown Jordan Services is recalling La-Z-Boy swivel patio chairs sold at Sears.com because the base can break during normal use, posing a fall hazard.
South Shore is recalling 5-drawer chests that pose tip-over and entrapment hazards to children if not anchored to the wall.
Van Hool is recalling specific 2010-2017 motorcoaches because the steering wheel may be difficult to turn in low temperatures, increasing crash risk.
Casual Living Worldwide is recalling about 2 million swivel patio chairs sold at Home Depot because the base can break, causing falls.
Teufelberger is recalling specific static ropes and throwlines because they are mislabeled as certified to NFPA safety standards, posing fall and injury risks to users.
IKEA is recalling MYSINGSÖ beach chairs because they can collapse, posing fall and fingertip amputation hazards. Consumers should stop using them and return them for a refund or replacement.