State
73,588 recalls have nationwide distribution and so reach Louisiana. 6,960 additional recalls listed Louisiana specifically in their distribution scope.
Of the 6,960 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 6,960 recalls whose distribution notice names Louisiana specifically. The 73,588 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
Mercedes-Benz is recalling certain 2020-2021 E-Class and AMG models due to a passenger seat limiter defect that may allow the seat to position too close to the frontal airbag, increasing injury risk during airbag deployment.
Polaris is recalling approximately 41,500 Ranger, ProXD, Gravely, and Bobcat off-road vehicles because a drive belt can break, damage the fuel line, and cause a fire.
Shyft Group is recalling certain 2021-2022 Spartan RV Chassis K1-K4 vehicles. A steering column defect may cause the steering output shaft to disengage, resulting in loss of steering control and crash risk.
Honda is recalling 2018-2020 Acura and Honda vehicles because the fuel pump may fail, causing the engine to stall while driving.
GM is recalling certain 2021 Chevrolet Tahoe vehicles because the second-row center seat belt latch may be trapped beneath the trim bezel. Passengers cannot use this seat belt, increasing injury risk in a crash.
General Motors is recalling 2015 Chevrolet Colorado and GMC Canyon vehicles because a poor electrical connection may cause loss of power steering, increasing crash risk.
General Motors is recalling certain 2017-2021 Chevrolet Camaro vehicles because the plastic 'Camaro' emblem on the steering wheel air bag cover may separate during air bag deployment, creating a projectile hazard.
KTM, Husqvarna, and GASGAS are recalling about 1,470 model year 2021 closed course competition motorcycles because the drive chain can break, posing a crash hazard.
Certain 2021 Ducati Multistrada V4 S motorcycles may have excessive valve guide wear that could break the valve head, decreasing engine performance and increasing crash risk. Ducati will replace the affected motorcycle engines at no cost.
Inyo Pool Products is recalling about 800 PureLine 1.5 HP pool pump motors because they can overheat and pose a fire hazard. No injuries have been reported.
Medtronic is recalling 4 units of Custom Perfusion Packs due to potentially elevated bacterial endotoxin levels that may cause acute inflammatory responses.
Merit Medical Systems is recalling 587 HeartSpan Transseptal Needles because the labeled tip curvature may not match the actual curvature, posing a risk of unintended anatomy puncture.
Medtronic is recalling 70 units of Affinity Pixie Cardiotomy/Venous Reservoirs due to potentially elevated bacterial endotoxin levels that may cause acute inflammatory responses.
Medtronic is recalling Affinity Pixie Oxygenators due to potentially elevated bacterial endotoxin levels that may cause acute inflammatory responses in patients.
Medtronic Perfusion Systems is recalling 7 units of the Custom Perfusion System because they may contain elevated levels of bacterial endotoxins, which can cause acute inflammatory responses in patients.
Medtronic is recalling 10 units of the Affinity Pixie Cardiotomy/Venous Reservoir due to potentially elevated bacterial endotoxin levels that may cause acute inflammatory responses.
Porsche is recalling 2021 Cayman, Boxster, and 718 Spyder vehicles because engine connecting rods may crack and loosen, increasing the risk of a crash or fire.
Jayco is recalling 2,144 motorhomes because a stove component may cause a gas leak, increasing the risk of fire.
Starcraft RV is recalling 2019-2020 travel trailers because an overtightened bolt may damage a seal, causing a gas leak that increases fire risk.
Medtronic is recalling 57 units of Affinity Pixie oxygenators due to potentially elevated bacterial endotoxin levels that may cause acute inflammatory responses.
Medtronic Perfusion Systems is recalling three units of its Custom Perfusion System because they may contain elevated levels of bacterial endotoxins. Patients exposed to these devices could develop an acute inflammatory response.
Merit Medical Systems is recalling Heartspan Transseptal Needles because the labeled tip curvature may not match the actual curvature, posing a risk of unintended anatomy puncture.
Bryant Ranch Prepack is recalling 35 bottles of Spironolactone 25 mg tablets because they may contain 50 mg tablets.
Medtronic is recalling 5 units of Affinity Pixie Cardiotomy Reservoirs due to potentially elevated bacterial endotoxin levels that may cause acute inflammatory responses.
Sagent Pharmaceuticals is recalling specific lots of Phenylephrine Hydrochloride Injection due to customer complaints of loose vial overseals that may compromise sterility.