State
73,741 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 73,741 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
Boy Story is recalling Mason and Billy action dolls because the vinyl joints can break, creating pieces that pose a choking hazard to young children.
Integrated Tower Systems is recalling 2007-2018 Mobile Tower trailers because a missing power disconnect on the control panel may cause electrical shock.
Honda is recalling 2010-2014 Ridgeline, Element, and Acura RL vehicles because the passenger air bag inflator may explode, posing a risk of serious injury or death.
Forest River is recalling 2019 Flagstaff and Rockwood recreational trailers because incorrectly oriented brake mounting flanges may cause premature brake failure, increasing crash risk.
Life Fitness is recalling about 11,800 PowerMill climbers because liquid entering the power receptacle can cause electrical arcing, sparking, and fire.
Honda is recalling specific 2010-2015 models because the passenger frontal air bag inflator may explode, potentially causing serious injury or death.
Honda is recalling 2019 Insight, Odyssey, and Ridgeline vehicles because a manufacturing error in the SRS control unit may prevent air bags or seatbelt pretensioners from deploying in a crash.
Honda is recalling 2017-2018 Civic and CR-V vehicles because a loose magnet in the electric power steering system may cause unintended steering input, increasing crash risk.
TerraTrike is recalling 600 adult tricycles because the right wheel hub mount can bend or break, creating a crash risk.
IKEA is recalling CALYPSO ceiling lamps because the glass shade can detach and fall, posing impact and laceration hazards. Consumers should stop using the lamps and return them for a refund or replacement.
QuVa Pharma is recalling 528 bags of Norepinephrine 4 mg in 5% Dextrose because the active ingredient may be missing. The product was distributed to hospitals nationwide.
Daimler Trucks North America is recalling 2017-2019 FCCC MC motorhome chassis because primary and secondary air lines were incorrectly connected to the pressure gauges, increasing crash risk.
Fresenius Medical Care is recalling 80 hemodialysis systems because a power failure during cleaning may allow disinfectant to remain in the machine and be delivered to patients.
Beaumont Bio-Med, Inc. is recalling 90 bottles of Sinus Response Homeopathic Formula due to manufacturing deviations that could result in microbial contamination.
Nova Bus is recalling 2017 LFS Hybrid and LFS Arctic Hybrid buses because pressure switches may fail, causing a loss of drive and increasing crash risk.
Degania Silicone is recalling 153 temperature sensor Foley catheters because defective sensors may display lower body temperatures than the patient's actual temperature.
Coviden is recalling temperature sensing Foley catheters that may display lower body temperature measurements than the patient's actual temperature.
Spartan Motors USA is recalling 2019 Spartan K2 Specialty vehicles because upper mounting fasteners may puncture the air spring bag, increasing crash risk.
Degania Silicone is recalling 89,122 Foley catheters with temperature sensors because defective sensors may display lower body temperatures than the patient's actual temperature.
EOS Imaging is recalling 17 sterEOS workstations because 3D projections may be incorrect when using specific secondary image captures, potentially leading to clinical errors.
Degania Silicone is recalling 4,332 Foley catheters with temperature sensors because defective sensors may display lower body temperatures than the patient's actual temperature.
bioMerieux is recalling VITEK 2 AST-P655 cards because six lots were manufactured with insufficient gentamicin, potentially affecting high-level resistance screening results.
Degania Silicone is recalling 330 Thermistor Foley catheters because defective sensors may display lower body temperatures than the patient's actual temperature.
Degania Silicone is recalling 500 units of temperature sensor Foley catheters because defective sensors may display lower body temperatures than the patient's actual temperature.
Fresenius Medical Care is recalling 40 units of the 2008T Hemodialysis System because a power failure during cleaning could leave disinfectant in the dialysate delivered to patients.