State
73,716 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 73,716 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
Ariston is recalling NTI and HTP residential gas boilers because a cracked condensate dish can cause fire, carbon monoxide poisoning, or impact injuries.
Harkla is recalling children's sensory swings because the ceiling hook can separate from its plate, posing a risk of serious injury from a fall.
DREO is recalling DR-HSH015 space heaters because they can overheat and ignite, posing fire and burn hazards. Consumers should stop using the heaters immediately.
Bodum USA is recalling 5.9 million French press coffee makers because damaged glass carafes can break during use, posing a risk of serious burn injuries.
Longjili Trading is recalling Pamag Pieeoo mattresses because they violate mandatory flammability standards, posing a risk of serious injury or death from fire.
PILLANI is recalling nursing pillows that violate safety standards and pose a risk of infant suffocation. Consumers should stop using them immediately and request a refund.
Yinklev is recalling Jocoevol 6-Drawer Dressers because they are unstable if not anchored to the wall, posing tip-over and entrapment hazards that can result in serious injury or death to children.
Whatever Works is recalling microwave grills because they can overheat and ignite, posing a risk of serious injury or death from fire.
HAIARA W5 PRO power banks are being recalled because their lithium batteries can explode and ignite, posing fire and burn risks.
SOOWERY is recalling 8-Drawer Fabric Dressers because they are unstable if not anchored to the wall, posing tip-over and entrapment risks to children.
RootStim is recalling three minoxidil hair regrowth products because the bottles lack required child-resistant packaging, posing a poisoning risk to young children.
QZH.DUAO children's pajama sets are being recalled because they violate mandatory safety standards, posing a risk of serious burn injuries.
Ventec Life Systems is recalling V+ Pro Emergency ventilators because an internal cable connector may disconnect, causing system reboots and interruption of ventilation therapy.
Greenwich Rx is recalling 4,319 vials of Glutathione Injection due to microbial contamination of sterile products. The affected lots were distributed nationwide.
Ventec Life Systems is recalling V*Home ventilators because an internal cable connector may disconnect, causing system reboots and interruption of therapy.
Beckman Coulter is recalling 336 SW41 rotors for Optima centrifuges due to a non-conforming microstructure that may cause the rotors to break during use.
EAK Distribution LLC is voluntarily recalling 3,600 packets of Heirloom Homegrown Green Sprouting Calabrese Broccoli Sprouts Seed due to a risk of Salmonella contamination.
Gardeners Basics is recalling Waltham 29 Broccoli Sprouting Seeds due to a Salmonella risk. The product was sold nationwide online.
Greiner Bio-One is recalling specific VACUETTE blood collection tubes due to EDTA contamination that may cause falsely elevated potassium and decreased calcium results.
Ventec Life Systems is recalling 325 VOCSN+Pro ventilators because an internal cable connector may disconnect, causing system reboots and interruption of ventilation therapy.
Shenzhen Techdow Pharmaceutical is recalling Heparin Sodium Injection due to a lack of assurance of sterility. The product was distributed nationwide in the USA.
Ventec Life Systems is recalling VCSN+Pro ventilators because an internal cable connector may disconnect, potentially interrupting ventilation therapy.
Pfizer is recalling 15,815 bottles of Levoxyl (levothyroxine sodium) 175 mcg tablets because stability testing confirmed the drug was subpotent.
Boston Scientific is recalling 1,442 Direxion Torqueable Microcatheters worldwide due to insufficient UV curing of the hydrophilic coating and raised ridges on nitinol sleeves.
Philips is recalling 13,206 Lumify Diagnostic Ultrasound Systems due to software and connection issues that may prevent scanning or disrupt function, potentially delaying diagnosis or treatment.