State
72,940 recalls have nationwide distribution and so reach Louisiana. 6,922 additional recalls listed Louisiana specifically in their distribution scope.
Of the 6,922 recalls naming Louisiana we have scored against our rubric, 1,094 (16%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 1,483 (21%) are Severe.
Which agencies issued them
These figures cover only the 6,922 recalls whose distribution notice names Louisiana specifically. The 72,940 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
Chrysler is recalling 2013-2016 Dodge Dart vehicles because the shifter cable may detach, preventing the car from shifting into park and increasing the risk of a crash.
Ford is recalling 2025 Ranger vehicles because the instrument panel top cover may prevent the passenger air bag from deploying as intended, increasing injury risk in a crash.
Chrysler is recalling specific Mopar Gear Shift Control Cables that may detach from the transmission, preventing the vehicle from shifting into park and increasing the risk of a crash.
Jayco is recalling 2026 Heartland Bighorn and North Point fifth wheel travel trailers because the murphy bed mechanism may fail, causing the bed to fall unexpectedly.
About 48,000 Living Glow five-in-one portable waist fans are being recalled because the lithium-ion batteries can overheat while charging; four fans have melted or caught fire.
Genesis Supreme RV is recalling one 2024 Supreme 28IKS fifth wheel trailer because the air conditioner soft start device may overheat and cause a fire.
Nissan is recalling 2013-2021 NV200 and 2015-2018 Chevrolet City Express vans because a misrouted sensor harness may damage wires, causing a short circuit that could stall the engine.
About 5,800 sets of 1,000 three-millimetre magnetic balls are being recalled because the loose high-powered magnets pose an ingestion hazard to children.
About 1,300 Bellabu Bear bamboo sherpa children's robes are being recalled because they violate the mandatory flammability standards for children's sleepwear.
About 920 Mom Genius retractable safety gates are being recalled because a child's torso can fit through the opening between the gate and the floor.
About 175,000 Scripto Premium Torch lighters are being recalled because they violate the mandatory safety standard for multipurpose lighters, posing fire and burn hazards.
About 740 Bmrwtg LED tutu skirts are being recalled because children can easily access the lithium coin batteries and the skirts lack the warnings required by Reese's Law.
About 490 YGJT baby loungers sold on SHEIN.com are being recalled because low sides, oversized foot openings and the lack of a stand create an unsafe infant sleeping environment.
Siemens is recalling one BIOGRAPH One (DE) system because an ice blockage in the magnet venting system could prevent helium escaping during a quench.
Medline is recalling 828 VALVE PACK-LF kits because they contain lots of cannula products where the catheter may not retain its shape.
Siemens is recalling 56 MAGNETOM Skyra fit MRI systems because an ice blockage in the magnet venting system could stop helium escaping during a quench.
Siemens is recalling 59 MAGNETOM Verio Dot systems because an ice blockage in the magnet venting system could stop helium escaping during a quench.
Medline is recalling 7,913 reprocessed ViewFlex Xtra ICE catheters because specific lots may carry small residual particulates on patient-contacting surfaces.
A MAGNETOM Connectom.X MRI system is being recalled because an ice blockage in the magnet venting system could prevent helium from escaping during a quench.
Medline is recalling 7,913 reprocessed Livewire Steerable Electrophysiology Catheters because specific lots may carry small residual particulates on patient-contacting surfaces.
Siemens is recalling 39 MAGNETOM Skyra Fit BioMatrix systems because an ice blockage in the magnet venting system could stop helium escaping during a quench.
Medline is recalling 7,913 reprocessed Webster CS 10-electrode catheters because specific lots may carry small residual particulates on patient-contacting surfaces.
Siemens is recalling 498 MAGNETOM Vida (DE) MRI systems because an ice blockage in the magnet venting system could stop helium escaping during a quench.
Medline is recalling 7,913 reprocessed Inquiry Steerable Diagnostic Catheters because specific lots may carry small residual particulates on patient-contacting surfaces.
Medline is recalling 7,913 reprocessed ACUSON AcuNav ultrasound catheters because specific lots may carry small residual particulates on patient-contacting surfaces.