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.
Airstream is recalling 2020-2021 Globetrotter travel trailers because adhesive on overhead cabinet doors may fail, causing the doors to fall and potentially injure occupants.
CFMOTO is recalling about 2,050 2021 CFORCE 800XC ATVs because the electronic power steering can malfunction, causing loss of control and posing a crash hazard.
Oshkosh is recalling 2021 S-Series vehicles because auxiliary axles may not be properly secured and could detach, increasing the risk of a crash.
Spartan Fire is recalling 2017-2020 Gladiator and MetroStar vehicles because a sealing washer may not seat correctly, causing a high-pressure fuel rail leak that increases fire risk.
Kidde is recalling about 226,000 TruSense smoke and combination smoke/carbon monoxide alarms because they may fail to alert consumers to a fire.
CareFusion 213, LLC is recalling ChloraPrep One-Step applicators because fungal growth breached package integrity. The product is a sterile skin antiseptic.
Golden Medal Mushroom Inc. is recalling Enoki Mushrooms after Michigan state sampling detected Listeria monocytogenes.
CareFusion 213, LLC is recalling Chloraprep One-Step antiseptic applicators because fungal growth breached package integrity. The product is distributed nationwide and internationally.
Peloton is recalling about 125,000 Tread+ treadmills because users, children, and pets can be pulled under the rear, causing injury or death.
CareFusion 213, LLC is recalling ChloraPrep One-Step applicators due to a lack of assurance of sterility. The product may allow fungal growth at labeled storage conditions, potentially breaching package integrity.
S & B Story LLC is recalling Imperial Extreme 2000 Capsules because FDA analysis found unapproved ingredients tadalafil and sildenafil.
CareFusion is recalling ChloraPrep antiseptic applicators because fungal growth breached package integrity. The product is non-sterile, but the breach compromises the sterility of the applicators.
Na Na Collection is recalling PremierZen Platinum 5000 capsules because FDA analysis detected unapproved active ingredients tadalafil and/or sildenafil.
Scott Fetzer Consumer Brands is recalling Wayne WaterBUG GLOW pumps because water exposure can cause short circuits, posing fire, burn, and electrical shock risks.
CareFusion 213, LLC is recalling ChloraPrep One-Step antiseptic applicators because fungal growth breached package integrity under labeled storage conditions.
Namoo Enterprise LLC is recalling PremierZen Black 5000 capsules because FDA analysis found unapproved ingredients tadalafil and sildenafil.
Na Na Collection is recalling Triple SupremeZen Gold 3500 capsules because FDA analysis found unapproved active ingredients tadalafil and/or sildenafil.
B&W Custom Truck Beds is recalling 5/8-inch stainless steel locking receiver hitch pins because the lock can be removed without a key, allowing the ball mount to detach.
Siemens is recalling 3,320 Artis angiography systems in the US because belt corrosion may cause system failure or unintended C-Arm movement.
Ford is recalling 2016-2019 Explorers because roof rail covers may detach, creating a road hazard and increasing crash risk.
Triple E RV is recalling specific 2020-2021 Unity, Wonder, and Serenity models because generator fan damage to wiring may cause electrical shock.
Torn & Glasser, Inc. is recalling Dark Chocolate Espresso Beans because the product contains walnuts that are not declared on the label.
B. Braun Medical is recalling 1,900 Filtered Triple-Leg Extension Sets because they may become occluded or unable to prime.
Luminex is recalling VERIGENE Processor SP units because they may produce false-negative results for specific enteric pathogens when used with the VERIGENE Enteric Pathogens Nucleic Acid Test Kit.
CareFusion 213, LLC is recalling ChloraPrep One-Step antiseptic applicators because fungal growth may breach package integrity. The product was distributed in the US and 12 other countries.