State
73,737 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 73,737 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
Subaru is recalling 2019 Crosstrek vehicles because the rear seat belt locking mechanism may not function as intended, increasing injury risk in crashes.
Altec is recalling 2016-2018 AT200A vehicles because incorrect rear tire markings may cause overloading, increasing crash risk.
Nissan is recalling 216,678 vehicles from 2011-2017 because the driver-side air bag inflator may rupture during deployment, potentially causing serious injury or death.
Bombardier is recalling 2020 Can-Am Spyder RT motorcycles because a brake support could break during emergency braking, causing total loss of braking ability.
BMW is recalling 2013-2016 328d xDrive vehicles because a driveline joint may fail, causing loss of rear power and increasing crash risk.
Chrysler is recalling 2019 Jeep Grand Cherokee and Dodge Durango vehicles because insufficiently hardened front differential pinion gears can wear down, leading to a loss of power or the PARK function.
Land Rover is recalling 2020 Range Rover Evoque vehicles because some headliners lack a required metal plate, potentially reducing head impact protection in a crash.
Daimler Vans USA is recalling 2019 Sprinter vans because the Operator's Manual may contain incorrect information about the automatic parking function, potentially increasing crash risk.
General Motors is recalling 2019-2020 Chevrolet Bolt EVs because a rear door cable may be too long, potentially causing the door to open unintentionally while driving.
Philips is recalling HeartStart MRx Monitor/Defibrillators because internal damage from drops or shocks may prevent therapy delivery, even if the device appears undamaged.
Chicago Indoor Garden, Inc. is recalling Sprout Salad 6 oz. because FDA analysis found E. coli and linked the product to an outbreak.
Chicago Indoor Garden is recalling Mixed Greens containing red clover sprouts because FDA testing found E. coli. The product was distributed nationwide, primarily through Whole Foods.
Chicago Indoor Garden, Inc. is recalling Red Clover products because FDA analysis found E. coli and linked the firm to an outbreak.
Med Man Distribution is recalling UP2 dietary supplements because FDA analysis found undeclared sildenafil, a prescription drug, in the product.
Chicago Indoor Garden, Inc. is recalling Spring Salad 6 oz. containing red clover sprouts because FDA testing found E. coli and linked the product to an outbreak.
Perrigo Company PLC is recalling specific lots of Regular Strength Acid Reducer, Ranitidine tablets, USP 75 mg, due to a CGMP deviation and possible contamination with the impurity N-nitrosodimethylamine.
CME America is recalling BodyGuard Infusion Pump Systems because they may deliver drugs at inaccurate rates, potentially causing faster or slower than expected medication administration.
Perrigo Company PLC is recalling Regular Strength Acid Reducer (Ranitidine) tablets due to a CGMP deviation and possible contamination with the impurity N-nitrosodimethylamine.
Perrigo Company PLC is recalling specific lots of Maximum Strength Acid Reducer, Cool Mint Ranitidine tablets due to a CGMP deviation and possible contamination with the impurity N-nitrosodimethylamine.
Med Man Distribution is recalling Bow & Arrow dietary supplements because they contain undeclared sildenafil, a prescription drug ingredient not listed on the label.
Perrigo Company PLC is recalling Maximum Strength Acid Reducer, Cool Mint Ranitidine tablets due to a CGMP deviation and possible contamination with the impurity N-nitrosodimethylamine.
Daimler Vans USA is recalling 2019 Freightliner and Mercedes-Benz Sprinter vans because a fender liner may chafe the brake hose, risking brake fluid loss and increased stopping distance.
Perrigo Company PLC is recalling Maximum Strength Acid Reducer, Cool Mint Ranitidine tablets due to a CGMP deviation and possible contamination with the impurity N-nitrosodimethylamine.
Perrigo Company PLC is recalling specific lots of Maximum Strength Acid Reducer, Ranitidine tablets, USP 150 mg, due to a CGMP deviation and possible contamination with the impurity N-nitrosodimethylamine.
Indian Motorcycle is recalling 2020 Challenger models because insufficient lubrication on the engine output shaft bearing could cause failure and sudden power loss.