State
73,806 recalls have nationwide distribution and so reach Louisiana. 6,966 additional recalls listed Louisiana specifically in their distribution scope.
Of the 6,966 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 6,966 recalls whose distribution notice names Louisiana specifically. The 73,806 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
Zimmer Biomet is recalling 5,947 Affixus Hip Fracture Nails because the set screw cannot advance or reverse from its original position.
Zimmer Biomet is recalling Affixus Hip Fracture Nails because the set screw cannot advance or reverse from its original position.
Zimmer Biomet is recalling Affixus Hip Fracture Nails because the set screw cannot advance or reverse from its original position.
Zimmer Biomet is recalling 5,947 Affixus Hip Fracture Nails because the set screw cannot advance or reverse from its original position.
Zimmer Biomet is recalling Affixus Hip Fracture Nails because the set screw cannot advance or reverse from its original position.
Zimmer Biomet is recalling Affixus Hip Fracture Nails because the set screw cannot advance or reverse from its original position.
Diagnostica Stago is recalling STA N¿oplastine¿ CI in-vitro diagnostic kits because quality control values fell outside assigned ranges, potentially affecting prothrombin time test results.
Micro Therapeutics is recalling 67 units of the ev3 TurboHawk Peripheral Plaque Excision System because packaged accessories are incompatible with the catheter, potentially preventing the removal of excised material.
Diagnostica Stago is recalling 24,043 kits of STA N¿oplastine¿ CI Plus reagents because quality control values fell outside assigned ranges, potentially affecting prothrombin time test results.
Pfizer is recalling 1,580 vials of Argatroban Injection because stability testing results were out of specification at the 18-month time point.
Par Pharmaceutical is recalling Pramipexole dihydrochloride extended release tablets because they contain a known impurity at levels exceeding specifications.
Ortho-Clinical Diagnostics is recalling VITROS Chemistry Products Cl- Slides because they do not meet maximum allowable interference claims for triglycerides in serum samples.
Ortho-Clinical Diagnostics is recalling VITROS Chemistry Products Cl- Slides because they do not meet maximum allowable interference claims for triglycerides.
Mylan Pharmaceuticals is recalling 656 bottles of Diltiazem HCl Extended-Release Capsules 120 mg because routine stability testing found out-of-specification related compounds.
Mylan Pharmaceuticals is recalling Diltiazem HCl Extended-Release Capsules 120 mg because routine stability testing revealed out-of-specification results for related compounds.
Forest River is recalling specific 2012-2018 buses because a wheelchair lift component may fail, allowing the platform to rise too high and increasing injury risk.
Dexter Axle is recalling specific Torsion Trailer Axles because incorrectly oriented brake mounting flanges may cause premature brake failure, increasing crash risk.
Volkswagen Group of America is recalling 2017-2018 Audi R8 Spyder and Coupe vehicles because transmission fluid may leak from the gearbox ventilation hose, creating a fire risk if it contacts hot engine parts.
Heil Environmental is recalling 2014-2016 garbage trucks because hydraulic oil tank brackets may crack, causing oil leaks that increase crash risk.
Trail King is recalling 2016-2018 ACS and AACS trailers because aluminum cross members may crack, potentially causing the suspension to loosen and increasing crash risk.
Chrysler is recalling 2017-2018 Alfa Romeo Giulia and 2018 Stelvio vehicles because engine misfires may overheat the catalytic converter, potentially causing a fire or engine stall.
Mazda is recalling 2009-2010 Mazda6 vehicles sold or registered in specific states because front cross member corrosion may weaken steering components, increasing crash risk.
Mitsubishi is recalling 2017-2018 Outlander, Outlander Sport, Eclipse Cross, and Outlander PHEV vehicles because incorrect software may prevent safety systems like automatic emergency braking from functioning.
Chrysler is recalling 2018-2019 Alfa Romeo Stelvio Quadrifoglio vehicles because an engine cooling hose may leak coolant, causing overheating and stalling.
Cruiser RV is recalling 2019 travel trailers because missing inner bearing races may cause hub failure and increase crash risk.