State
73,817 recalls have nationwide distribution and so reach Tennessee. 7,860 additional recalls listed Tennessee specifically in their distribution scope.
Of the 7,860 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 1,974 (25%) are Severe.
Which agencies issued them
These figures cover only the 7,860 recalls whose distribution notice names Tennessee specifically. The 73,817 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
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.
Oscor, Inc. is recalling ATAR Reusable Extension Cables because they may separate from the connector during use, posing a risk to patients.
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.
Teva Pharmaceuticals is recalling 360 bottles of Paliperidone Extended-Release Tablets because one tablet failed a routine stability test for drug release.
Baxter Healthcare is recalling 54,528 bags of 5% Dextrose Injection because the bags may leak, compromising sterility.
Oscor, Inc. is recalling ATAR Disposable Extension Cables because they may separate from the connector during use, posing a risk to patients.
Bristol-Myers Squibb is recalling 48,180 bottles of Eliquis 5mg tablets because one bottle was found to contain 2.5mg tablets instead.
Daimler Trucks is recalling specific 2017-2018 Freightliner and Western Star trucks because a fuel pump drive gear may slip, causing sudden engine stalls and increasing crash risk.
Advanced Pharma Inc. is recalling QUELICIN (Succinylcholine Chloride) Injection due to a lack of assurance of sterility. The recall affects 2,350 units distributed nationwide.
Advanced Pharma Inc. is recalling 72 units of Potassium Phosphate IV bags nationwide due to a lack of assurance of sterility.
Advanced Pharma Inc. is recalling specific lots of Potassium Phosphate in 0.9% Sodium Chloride bags because the company cannot assure the product's sterility.
O-Two Medical Technologies is recalling Adult Ventilation Timers because the flash rate may be twice the labeled rate, potentially affecting ventilation guidance.
Natus Neurology is recalling 2,335 Elite 5 MHz Vascular Probes because excessive background noise may mask heart rate and blood flow signals.
St. Jude Medical is recalling 373 Infinity 7 Implantable Pulse Generators because exposure to monopolar electrosurgical devices may cause a loss of neuromodulation therapy.