State
73,741 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 73,741 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
LivaNova is recalling Perfusion Tube Sets because included Medtronic display sets may have packaging pinholes, creating a risk of sterile barrier breach.
LivaNova is recalling Perfusion Tube Sets because included Medtronic display sets may have pinholes in their packaging, creating a potential sterile barrier breach.
LivaNova is recalling Perfusion Tube Sets because included Medtronic display sets may have pinholes in their packaging, creating a risk of sterile barrier breach.
LivaNova is recalling Perfusion Tube Sets because included Medtronic display sets may have pinholes in their packaging, creating a risk of sterile barrier breach.
NatureBox is recalling Sticks 'n Stones snack mix because a consumer found a peanut in a product that does not list peanuts as an ingredient.
Olympus is recalling 146 VANTA Analytical X-Ray Systems because they may fail to stop testing when no sample is present.
LivaNova is recalling Perfusion Tube Sets because included Medtronic display sets may have packaging pinholes, creating a potential sterile barrier breach.
LivaNova is recalling Perfusion Tube Sets because the included Medtronic display sets may have pinholes, creating a potential sterile barrier breach.
LivaNova is recalling Perfusion Tube Sets because the included Medtronic display sets may have pinholes, creating a potential sterile barrier breach.
LivaNova is recalling Perfusion Tube Sets because included display sets may have packaging pinholes that compromise sterility.
LivaNova is recalling Perfusion Tube Sets because included display sets may have packaging pinholes that compromise sterility.
LivaNova is recalling Perfusion Tube Sets because included Medtronic display sets may have packaging pinholes that compromise sterility.
Dr. Reddy's Laboratories is recalling specific lots of Pravastatin Sodium tablets because they failed impurity specifications.
Stryker Neurovascular is recalling 43 Stroke Fast Packs because the carton sleeve labels did not match the physical contents inside the packs.
Quidel Corporation is recalling InflammaDry sample collectors because in-house testing found plastic spurs at the tips of some units.
Bayer HealthCare is recalling Alka-Seltzer Gold effervescent tablets because customer complaints confirmed small holes or cracks in the foil of the blister packs.
Teva Pharmaceuticals USA is recalling 28,188 bottles of Famotidine 20 mg tablets because they failed tablet weight specifications.
Sentinel CH SPA is recalling MULTIGENT Creatinine (Enzymatic) reagents because Reagent 1 may cause quality control values to shift out of acceptable range.
Zydus Pharmaceuticals is recalling Divalproex Sodium Delayed Release Tablets because they failed to meet dissolution specifications.
Xintec Corp is recalling OptiLITE laser surgery products because reprocessing instructions may not meet new standards for cleaning and sterilization.
Stryker Neurovascular is recalling 48 Stroke Fast Packs because the pre-printed carton sleeve contents did not match the physical items inside.
Bayer is recalling Alka-Seltzer Extra Strength effervescent tablets because customer complaints confirmed small holes or cracks in the foil blister packs.
Stryker Neurovascular is recalling 139 Stroke Fast Packs because the pre-printed contents on the carton sleeve did not match the physical contents of the pack.
Stryker Neurovascular is recalling 63 Stroke Fast Packs because the printed carton contents did not match the physical items inside.
Time-Cap Laboratories is recalling 1,980 bottles of 600 mg ibuprofen tablets because some bottles contained 800 mg tablets.