State
73,722 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 73,722 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
Red Mountain Compounding Pharmacy is recalling specific vials of Magnesium Sulfate Injection because the FDA determined there is a lack of assurance of sterility.
Red Mountain Compounding Pharmacy is recalling S-E2/TEST CYP 0.4MG/1MG/MLMDV IN OIL INJECTION vials due to a lack of assurance of sterility.
Red Mountain Compounding Pharmacy is recalling specific lots of zinc sulfate solution because the FDA could not ensure the product was sterile.
Red Mountain Compounding Pharmacy is recalling benzalkonium chloride solution because the product lacks assurance of sterility.
Red Mountain Compounding Pharmacy is recalling S-Hydroxyprogesterone Caproate injections due to a lack of assurance of sterility.
Red Mountain Compounding Pharmacy is recalling S-MIC 25/50/50mg/ml Cyanocobalamin 1mg/ml MDV Solution due to a lack of assurance of sterility.
Red Mountain Compounding Pharmacy is recalling S-Hydroxyprogesterone Caproate injections due to a lack of assurance of sterility.
Red Mountain Compounding Pharmacy is recalling S-Levocarnitine 100mg/mL injection vials because the FDA identified a lack of assurance of sterility.
Teleflex is recalling Babi.Plus 12.5 cm H2O Pressure Relief Manifolds because the devices vented gas below the stated pressure.
Red Mountain Compounding Pharmacy is recalling specific lots of Vitamin D3 10,000 IU/mL oil injection due to a lack of assurance of sterility.
Red Mountain Compounding Pharmacy is recalling S-HCG/B12A injection vials due to a lack of assurance of sterility. The recall affects 11 vials distributed nationwide.
Red Mountain Compounding Pharmacy is recalling S-Atropine 0.5% ophthalmic solution due to a lack of assurance of sterility.
Medtronic is recalling MiniMed Model 500 Remote Controls used with the MiniMed 508 Insulin Pump due to a potential security vulnerability.
Red Mountain Compounding Pharmacy is recalling S-Dextrose/Glycerin/Phenol injection vials due to a lack of assurance of sterility. The product was distributed nationwide.
Red Mountain Compounding Pharmacy is recalling specific lots of Magnesium Chloride Injection because the FDA identified a lack of assurance of sterility.
Red Mountain Compounding Pharmacy is recalling S-Lysine HCL 100mg/mL vials because the FDA cannot ensure the product is sterile.
Philips Medical Systems is recalling 1,167 Forte Gamma Camera Systems because a detector may fall unimpeded to the end stops of its travel limit.
Red Mountain Compounding Pharmacy is recalling specific lots of S-Glutathione 200mg/mL vials due to a lack of assurance of sterility.
Red Mountain Compounding Pharmacy is recalling S-TEST CYP 25mg/ml vials nationwide due to a lack of assurance of sterility.
Red Mountain Compounding Pharmacy is recalling S-Calcium Glucunate 1% Opth Irrigation due to a lack of assurance of sterility. The product was distributed nationwide.
Red Mountain Compounding Pharmacy is recalling S-Hyaluronidase 150U/mL injection vials because the product lacks assurance of sterility.
Red Mountain Compounding Pharmacy is recalling specific lots of Potassium Chloride Injection because the FDA identified a lack of assurance of sterility.
Red Mountain Compounding Pharmacy is recalling S-Phenol 6% Injection Solution because the product lacks assurance of sterility.
Red Mountain Compounding Pharmacy is recalling S-E2/Test Cyp 1mg/4mg sesame oil injections due to a lack of assurance of sterility.
Red Mountain Compounding Pharmacy is recalling S-B5/B6/B12M solution vials because the FDA cannot ensure the product is sterile.