State
73,827 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 73,827 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
Infiniti Creations is voluntarily recalling HCG Drops due to misbranding and potential undeclared HCG content.
Merit Medical Systems is voluntarily recalling 107,341 Fluid Administration Sets due to a molding defect in the drip chamber.
Synthes (USA) Products LLC is recalling 319 sterile 3.0 mm Guide Rods because their peel pouches are delaminating.
Zydus Pharmaceuticals USA Inc. is recalling BUPROPION Hydrochloride Extended-Release Tablets, 300 mg, because the product failed to meet dissolution specifications at an intermediate time point.
Infiniti Creations, LLC is voluntarily recalling A New You HCG Drops due to misbranding and potential undeclared HCG content.
Synthes (USA) Products LLC is recalling 139 units of 2.5 mm Guide Rods because their sterile peel pouches are delaminating.
Infiniti Creations, LLC is voluntarily recalling SkinEHCG HCG Drops due to misbranding and potential undeclared HCG content.
Infiniti Creations, LLC is voluntarily recalling Original HCG Drops due to misbranding and potential undeclared HCG content.
Infiniti Creations, LLC is voluntarily recalling HCG Plus drops due to misbranding and potential undeclared HCG content.
Sun Pharmaceutical Industries is recalling KENALOG (Triamcinolone Acetonide) Spray due to low alcohol content. The product failed stability specifications.
Synthes (USA) Products LLC is recalling 1,951 sterile 2.5 mm reaming rods because their peel pouches are delaminating.
Mylan Pharmaceuticals is recalling Diltiazem HCl Extended-Release Capsules because of out-of-specification results for a known compound.
Synthes (USA) Products LLC is recalling 5,478 sterile 3.0 mm reaming rods because their peel pouches are delaminating.
West-Ward Pharmaceuticals is recalling 32,102 bottles of Amoxicillin oral suspension because some bottles are missing the color-coded panel that displays the product strength.
Infiniti Creations, LLC is voluntarily recalling Supervision Weightloss HCG Drops due to misbranding and potential undeclared HCG content.
Van Hool is recalling specific motorcoaches because front steering knuckle carriers may crack, potentially causing a wheel to separate and increasing crash risk.
Gree Electric Appliances is recalling approximately 2.5 million dehumidifiers sold under various brands because they can overheat and catch fire, posing serious fire and burn hazards.
Stanley is recalling about 70,000 commercial door locksets because the latches can fail, preventing doors from being unlocked from the inside during an emergency.
Toyota is recalling 2011-2016 Sienna minivans because the power sliding door may open unexpectedly while the vehicle is moving, increasing the risk of injury to occupants.
Forest River is recalling 2016-2017 StarTrans PS2 buses because the instrument cluster may display 'PARK' instead of 'BRAKE' during a brake malfunction, increasing crash risk.
Johnson Health Tech is recalling Matrix ClimbMills because the stop/pause controls can malfunction, posing a fall hazard to users.
Autocar is recalling 2013-2017 Xpeditor vehicles because fuse box vibration may cause the ignition relay to open, leading to an engine stall and increased crash risk.
Midwest Automotive Designs is recalling 2016 Mercedes-Benz Sprinter 2500 and 3500 vans because certain left seat adjusters may allow seats to move during a crash.
Autocar is recalling 2012-2016 Xpeditor vehicles because hybrid power drive unit bolts may not be tightened properly, risking detachment and crashes.
Maserati is recalling 326 model year 2017 Quattroporte and Ghibli vehicles because a loose rear differential pinion nut may cause the rear wheels to lock up, increasing crash risk.