State
73,817 recalls have nationwide distribution and so reach Oklahoma. 5,823 additional recalls listed Oklahoma specifically in their distribution scope.
Of the 5,823 recalls naming Oklahoma we have scored against our rubric, 1,040 (18%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 1,494 (26%) are Severe.
Which agencies issued them
These figures cover only the 5,823 recalls whose distribution notice names Oklahoma specifically. The 73,817 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
FDA is recalling Ultimate Body Tox PRO capsules because they contain undeclared sibutramine, a controlled substance removed from the market for safety reasons.
Simply Fresh Fruit is recalling cantaloupe and fruit mixes with cantaloupe because they may be contaminated with Listeria monocytogenes.
Simply Fresh Fruit is recalling specific cantaloupe and fruit mix products because they may be contaminated with Listeria monocytogenes.
Woodland Foods is recalling Smashburger Autumn Harvest Salad Topper because sunflower seeds used in the product may be contaminated with Listeria.
Simply Fresh Fruit is recalling 276 pails of 1 GL CVF Cantaloupe Chunks because they may be contaminated with Listeria monocytogenes.
Hospira Inc. is recalling 143,250 vials of Bupivacaine Hydrochloride Injection due to a confirmed report of particulate matter in a single vial.
Simply Fresh Fruit is recalling cantaloupe and fruit mixes with cantaloupe because they may be contaminated with Listeria monocytogenes.
Love My Tru Body is recalling Skinny Bee Diet capsules because they contain undeclared sibutramine, desmethylsibutramine, and phenolphthalein.
Woodland Foods is recalling Di Bruno Bros Roasted & Salted Sunflower Seeds due to potential Listeria contamination. The product was distributed to food distributors in 25 states.
Simply Fresh Fruit is recalling cantaloupe and fruit mixes in grape juice because they may be contaminated with Listeria monocytogenes.
Simply Fresh Fruit is recalling cantaloupe and fruit mixes with cantaloupe because they may be contaminated with Listeria monocytogenes.
Woodland Foods is recalling D'Allesandro Almond Trail Mix because sunflower seeds in the product may be contaminated with Listeria.
Woodland Foods is recalling D'Allesandro Roasted Salted Sunflower Seeds due to potential Listeria contamination. The product was distributed to food distributors in 26 states.
Simply Fresh Fruit is recalling cantaloupe and fruit mixes containing cantaloupe because they may be contaminated with Listeria monocytogenes.
Woodland Foods is recalling salt-free roasted sunflower seeds potentially contaminated with Listeria. The product was distributed to food distributors in 25 states.
Impax Laboratories is recalling 3,074 boxes of Lamotrigine Orally Disintegrating Tablets because some 200 mg boxes contained 100 mg tablets.
Virtus Pharmaceuticals is recalling 24,444 bottles of Hyoscyamine Sulfate tablets because they failed content uniformity specifications, resulting in inconsistent drug potency.
Nissan is recalling 509 2017 Infiniti QX30 vehicles because the passenger air bag inflator may fail to ignite, preventing deployment during a crash.
Simply Fresh Fruit is recalling cantaloupe and fruit mixes with cantaloupe because they may be contaminated with Listeria monocytogenes.
Woodland Foods is recalling D'Allesandro Salt-Free Roasted Sunflower Seeds due to potential Listeria contamination. The product was distributed to food distributors in 26 states.
Making It a Lifestyle is recalling 3rd Degree capsules because they contain undeclared sibutramine and were marketed without an approved NDA or ANDA.
Virtus Pharmaceuticals is recalling Hyoscyamine Sulfate tablets because they failed content uniformity specifications, resulting in both superpotent and subpotent doses.
Chaos and Pain is recalling its Cannibal Ferox Amped pre-workout supplement because it contains an undeclared prohibited substance.
Naturecom is recalling 500g bags of DMAA powder because the product may contain 1,3-dimethylamylamine. The recall covers products distributed nationwide and internationally.
The FDA is recalling Ultroid Hemorrhoid Management Systems because they were not manufactured under required quality system controls.