State
73,722 recalls have nationwide distribution and so reach Louisiana. 6,965 additional recalls listed Louisiana specifically in their distribution scope.
Of the 6,965 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 1,739 (25%) are Severe.
Which agencies issued them
These figures cover only the 6,965 recalls whose distribution notice names Louisiana specifically. The 73,722 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
Ananda Apothecary is recalling four essential oil products because their packaging is not child-resistant, posing a risk of poisoning if swallowed by young children.
Miracle Botanicals is recalling Wintergreen and Birch Essential Oils because the packaging is not child-resistant, posing a risk of poisoning if swallowed by young children.
Cooper Lighting is recalling about 39,000 All Field and Prism RGBA light fixtures because lenses can loosen and fall, posing an injury risk to people below.
DaVinci is recalling about 3,000 Bailey bassinets because the mattress support can disengage, posing fall and entrapment risks to infants.
Beyond Better Foods is recalling Enlightened Dairy-Free Chocolate Peanut Butter Frozen Dessert because it may contain undeclared milk.
Mount Franklin Foods is recalling 7-Select Yogurt Pretzels because they may contain undeclared peanuts. The product was distributed to 7-11 stores nationwide.
Beaming White LLC is recalling Koala Hand Sanitizer because the ethanol content is below the label claim and undeclared isopropyl alcohol is present.
LivaNova USA Inc. is recalling 150 units of Vein Irrigation Cannulas with blunt tips because internal tests identified potential breaches in the sterile barrier.
Beaming White LLC is recalling Koala Hand Sanitizer because the ethanol level is below the label claim and it contains undeclared isopropyl alcohol.
The Harvard Drug Group is recalling Metformin Hydrochloride Extended-Release Tablets due to potential NDMA impurity levels above established limits.
Beaming White LLC is recalling Koala Hand Sanitizer because the active ingredient ethanol was tested below the label claim and undeclared isopropyl alcohol was present.
Trident Seafoods is recalling Gordon Choice Imitation Crab Supreme Style because the product may contain undeclared egg white.
Kia is recalling 2020 Sedona vehicles because a loose alternator terminal nut may cause electrical arcing and increase the risk of a fire.
LivaNova USA Inc. is recalling 600 units of sterile disposable connectors because internal tests found the sterile barrier may be breached.
LivaNova USA Inc. is recalling specific lots of sterile disposable connectors because internal tests found potential breaches in the sterile barrier.
Brill Inc. is recalling 252 cases of frozen cookie dough because the product may contain undeclared walnuts, a major food allergen.
LivaNova USA Inc. is voluntarily recalling 220 units of 3/8 inch Y connectors due to a Class II defect.
LivaNova USA Inc. is recalling 240 units of sterile standalone connectors because internal tests found potential breaches in the sterile barrier.
LivaNova USA Inc. is recalling specific lots of sterile disposable connectors because internal tests found potential breaches in the sterile barrier.
Elekta is recalling 51 Leksell Vantage Stereotactic Systems because the locking mechanism at the Instrument Carrier and Arc interface may not function properly.
Siemens Healthcare Diagnostics is recalling CentraLink Data Management System software versions 16.0.2 and 16.0.3 due to a defect that may cause erroneous patient results.
LivaNova USA Inc. is recalling 768 units of Sterile Disposable Connectors because internal tests found potential breaches in the sterile barrier.
Lidl US is recalling approximately 1,840 Silvercrest bread makers because the lid can become energized, posing an electric shock hazard.
LivaNova USA Inc. is recalling 120 units of sterile disposable connectors because internal tests found the sterile barrier may be breached.
Preventice Services is recalling eight BodyGuardian Heart Remote Monitoring Kits because unvalidated software may cause inaccurate data collection, making patient reports unreliable for condition evaluation.