State
73,833 recalls have nationwide distribution and so reach Louisiana. 6,967 additional recalls listed Louisiana specifically in their distribution scope.
Of the 6,967 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 1,740 (25%) are Severe.
Which agencies issued them
These figures cover only the 6,967 recalls whose distribution notice names Louisiana specifically. The 73,833 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
Chrysler is recalling 2014-2016 RAM ProMaster and 2015-2016 ProMaster City vehicles because a software error may prevent trailer brake lights from illuminating, increasing crash risk.
General Motors is recalling certain 2013-2016 Chevrolet Sonic, Trax, and Spark vehicles because the radio software may fail to provide an audible warning chime, increasing the risk of vehicle theft.
Mevion Medical Systems is recalling five MEVION S250 proton therapy systems because an aperture may fall out during gantry motion, posing a risk of traumatic injury or death to patients.
Impax Laboratories is recalling 67,428 bottles of Dextroamphetamine Sulfate Tablets USP, 10 mg, because the product failed impurities and degradation specifications.
Ford is recalling specific 2011-2012 F-150, Mustang, Expedition, and Navigator vehicles because the automatic transmission may unexpectedly downshift to first gear, increasing crash risk.
Boston Scientific is recalling Fetch 2 Aspiration Catheters because the catheter shafts may break, potentially requiring additional procedures to remove the broken piece from patients.
Ford is recalling 2016 Fusion vehicles because the driver seat track may be improperly welded, potentially failing to restrain the driver in a crash.
Chrysler is recalling 2016 Jeep Grand Cherokee vehicles because a loose electrical connection in the brake transmission shift interlock solenoid may cause the transmission to lock in Park or Neutral.
Hospira Inc. is recalling 81,888 bags of Potassium Chloride Injection due to potential contamination with an aromatic hydrocarbon resin.
Acorn Stairlifts Inc is recalling 1,290 Acorn 180 Curved Stairlifts in the US because aluminum rivets may break under prolonged use.
Hospira Inc. is recalling 4,368 bags of Dextrose Injection, USP, 50% due to potential contamination with an aromatic hydrocarbon resin.
Hospira Inc. is recalling 552 bags of Dextrose Injection, USP, 20% due to potential contamination with an aromatic hydrocarbon resin.
Impax Laboratories is recalling specific lots of Dextroamphetamine Sulfate Tablets because they failed impurity and degradation specifications.
Ossur H / F is recalling Lil Angel Vest P3 Sorbatex units because the plastic stabilizer strap may partially or completely fracture.
Subaru is recalling 766 model year 2015 Legacy and Outback vehicles because excess moisture in the brake fluid may impair the electronic stability control system, increasing crash risk.
Siemens Medical Solutions is recalling 1,096 CT systems due to software bugs that may cause scan aborts, rescans, or accidental x-radiation.
Ossur H / F is recalling Lil Angel Vest P2 Sorbatex pediatric vests because the plastic stabilizer strap may partially or completely fracture.
Ossur H / F is recalling Lil Angel Vest P3 Kodel units due to a potential for partial or complete fracture of the plastic stabilizer strap.
Siemens Medical Solutions is recalling 1,096 CT systems due to software bugs that may cause scan aborts, rescans, or accidental radiation.
Hospira Inc. is recalling 22,292 bags of Mannitol I.V. 20% due to potential contamination with an aromatic hydrocarbon resin.
Stryker Howmedica Osteonics Corp. is recalling 118 units of the VariAx Compression Plating System because bone screws may pass through oblong holes during insertion.
Siemens Medical Solutions USA is recalling 1,096 SOMATOM Definition CT systems due to software bugs that may cause scan aborts, re-scans, or accidental radiation.
Ossur H / F is recalling Lil Angel Vest P2 Lambswool units because the plastic stabilizer strap may partially or completely fracture.
Ossur H / F is recalling 435 Lil Angel Vest P2 Kodel units due to a potential for partial or complete fracture of the plastic stabilizer strap.
Siemens is recalling 1,096 SOMATOM Definition AS CT systems due to software bugs that may cause scan aborts, rescans, or accidental radiation.