State
73,718 recalls have nationwide distribution and so reach Tennessee. 7,859 additional recalls listed Tennessee specifically in their distribution scope.
Of the 7,859 recalls naming Tennessee we have scored against our rubric, 1,324 (17%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 1,973 (25%) are Severe.
Which agencies issued them
These figures cover only the 7,859 recalls whose distribution notice names Tennessee specifically. The 73,718 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
Life Technologies is recalling 16 Ion Torrent Genexus Dx systems due to software vulnerabilities. The affected units are distributed in 11 US states.
Boston Scientific is recalling 1,135 units of Direxion Torqueable Microcatheters due to insufficient UV curing of the hydrophilic coating and raised ridges on nitinol sleeves.
Boston Scientific is recalling 8,542 Direxion Torqueable Microcatheters due to insufficient UV curing of the hydrophilic coating and raised ridges on nitinol sleeves.
Boston Scientific is recalling 1,212 Direxion Torqueable Microcatheters due to insufficient UV curing of the hydrophilic coating and raised ridges on nitinol sleeves.
Pritam International is voluntarily recalling 797,868 tubes of Brush Buddies toothpaste nationwide due to CGMP deviations.
Boston Scientific is recalling 860 Direxion Torqueable Microcatheters due to insufficient UV curing of the hydrophilic coating and raised ridges on nitinol sleeves.
Evexias Health Solutions is recalling Amino Ultra dietary supplements because the product is mislabeled and fails to declare fish oil.
Medline Industries is recalling 161 units of Drape C-SEC Fen Clear Screen Wire because the product is difficult to remove and leaves adhesive residue on patient skin.
Boston Scientific is recalling 926 Direxion Torqueable Microcatheters due to insufficient UV curing of the hydrophilic coating and raised ridges on nitinol sleeves.
Pritam International is voluntarily recalling 320,232 tubes of Brush Buddies toothpaste nationwide due to Current Good Manufacturing Practice (CGMP) deviations.
Boston Scientific is recalling 126 Direxion Torqueable Microcatheters due to insufficient UV curing of the hydrophilic coating and raised ridges on nitinol sleeves.
Pritam International is voluntarily recalling Brush Buddies My Little Pony toothpaste due to Current Good Manufacturing Practice (CGMP) deviations.
Boston Scientific is recalling 112 Direxion Torqueable Microcatheters due to insufficient UV curing of the hydrophilic coating and raised ridges on nitinol sleeves.
Boston Scientific is recalling 86 Direxion Torqueable Microcatheters due to insufficient UV curing of the hydrophilic coating and raised ridges on nitinol sleeves.
Pritam International is voluntarily recalling 389,880 tubes of evo Sensitive Anticavity Fluoride Toothpaste due to CGMP deviations.
Boston Scientific is recalling 39 units of Direxion Torqueable Microcatheters due to insufficient UV curing of the hydrophilic coating and raised ridges on nitinol sleeves.
Medline is recalling 222 C-Section Pack kits because they are difficult to remove and leave adhesive residue on patient skin.
Boston Scientific is recalling 486 units of Direxion Torqueable Microcatheters due to insufficient UV curing of the hydrophilic coating and raised ridges on nitinol sleeves.
Boston Scientific is recalling 598 Direxion Torqueable Microcatheters due to insufficient UV curing of the hydrophilic coating and raised ridges on nitinol sleeves.
Boston Scientific is recalling 658 units of Direxion Torqueable Microcatheters due to insufficient UV curing of the hydrophilic coating and raised ridges on nitinol sleeves.
Strides Pharma Inc. is recalling 49,488 bottles of Cinacalcet Tablets, 30 mg, because they failed dissolution specifications. The recall is classified as Class II.
Pritam International is voluntarily recalling 409,800 tubes of Brush Buddies Barbie toothpaste due to Current Good Manufacturing Practice (CGMP) deviations.
Boston Scientific Cork, Ltd. is recalling 609 units of Direxion Torqueable Microcatheters due to insufficient UV curing of the hydrophilic coating and raised ridges on nitinol sleeves.
Boston Scientific is recalling 357 Direxion Torqueable Microcatheters due to insufficient UV curing of the hydrophilic coating and raised ridges on nitinol sleeves.
Medline Industries is recalling C-section drapes with pouches because they are difficult to remove and leave adhesive residue on patient skin.