State
73,817 recalls have nationwide distribution and so reach Louisiana. 6,966 additional recalls listed Louisiana specifically in their distribution scope.
Of the 6,966 recalls naming Louisiana we have scored against our rubric, 1,107 (16%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 1,740 (25%) are Severe.
Which agencies issued them
These figures cover only the 6,966 recalls whose distribution notice names Louisiana specifically. The 73,817 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
Spartan Motors is recalling 2015-2017 Utilimaster Aeromaster vehicles because a missing ground wire may cause intermittent loss of windshield wiper function, increasing crash risk.
Manhattan Toy is recalling Winkel Colorburst activity toys because plastic tubes can break into small pieces, posing a choking hazard to infants.
Smeal is recalling 2016-2017 Aerial Fire Apparatus vehicles because a hydraulic manifold may not be fully seated, causing fluid leaks and potential injury.
Organic Herbal Supply is recalling ZRECT for Women herbal capsules because FDA testing found undeclared prescription drugs, including tadalafil and sildenafil.
Organic Herbal Supply is recalling UPROAR male enhancement capsules because FDA testing found undeclared prescription drugs, including tadalafil and sildenafil.
Wildway LLC is recalling specific lots of Coconut Cashew Grain-free Granola due to potential contamination with Listeria monocytogenes.
Organic Herbal Supply is recalling Rectalis Male Enhancement Capsules because FDA analysis found undeclared prescription drugs, including tadalafil and sildenafil.
Organic Herbal Supply is recalling Xrect Male Enhancement capsules because FDA analysis found undeclared prescription drugs tadalafil, sildenafil, and Flibanserin.
Organic Herbal Supply is recalling Enhancerol Herbal Dietary Supplement Capsules because FDA analysis found undeclared tadalafil, sildenafil, and Flibanserin.
Organic Herbal Supply is recalling Tornado Male Enhancement capsules because FDA analysis found undeclared prescription drugs, including tadalafil and sildenafil.
Organic Herbal Supply is recalling ZDaily Testosterone and Libido Booster capsules because FDA analysis found undeclared prescription drugs, including tadalafil, sildenafil, and flibanserin.
Kroger is recalling Simple Truth Dry Roasted Macadamia Nuts due to an expanded supplier notification regarding Listeria monocytogenes.
Organic Herbal Supply is recalling LabidaMAX Herbal Dietary Supplement Capsules because FDA analysis found undeclared prescription drugs.
Organic Herbal Supply is recalling BIGnHARD Male Enhancement Capsules because FDA testing found undeclared prescription drugs, including tadalafil and sildenafil.
Organic Herbal Supply is recalling Cummor Natural Male Enhancement capsules because FDA analysis found undeclared prescription drugs, including tadalafil and sildenafil.
Organic Herbal Supply is recalling ZRECT Male Enhancement capsules because FDA analysis found undeclared prescription drugs, including tadalafil and sildenafil.
Wildway LLC is recalling specific lots of Apple Cinnamon Grain-Free Granola due to potential Listeria monocytogenes contamination.
Advanced Pharma Inc. is recalling specific lots of Potassium Phosphate Injection due to a lack of assurance of sterility. The product was distributed nationwide.
Wildway LLC is recalling 434 cases of Banana Nut Grain-free Granola due to potential Listeria monocytogenes contamination. The product was distributed nationwide.
Polaris is recalling about 25,600 model year 2014 Sportsman 570 ATVs because fuel can leak into the headlight pod, posing fire hazards.
Wildway LLC is recalling specific lots of Trader Joe's Grainless Granola due to potential contamination with Listeria monocytogenes.
Wildway LLC is recalling 442 cases of Vanilla Bean Espresso Grain-free Granola due to potential Listeria monocytogenes contamination.
AstraZeneca is recalling 40,368 bottles of BRILINTA 90 mg tablets because some bottles contained foreign Zurampic tablets.
SCA Pharmaceuticals is recalling 660 bags of Potassium Phosphate IV solution due to a lack of sterility assurance. The product was distributed in LA, PA, NY, and WI.
Baxter Healthcare is recalling 0.9% Sodium Chloride Injection bags due to customer complaints about leaking bags, which raises concerns about the product's sterility.