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.
Ford is recalling 2018 F53 stripped chassis vehicles because improperly heat-treated front wheel studs may break, increasing crash risk.
Keystone RV Company is recalling 2018-2019 Dutchmen Aerolite trailers because the safety chains are rated lower than the trailer's weight, increasing crash risk if detached.
Volkswagen is recalling 2018 Tiguan vehicles because the panoramic sunroof LED module may short circuit, increasing the risk of a fire.
Forest River is recalling 2019 Palomino hardside truck campers because the Federal Placard lists an incorrect dry weight, which may result in the vehicle being overloaded.
Chrysler is recalling specific 2014-2018 Chrysler 300, Dodge Charger, and Challenger vehicles because a defect may prevent the cruise control system from disengaging.
Allura Imports is recalling about 64,000 children's pajamas and onesies because they fail to meet federal flammability standards, posing a burn risk.
Multiquip is recalling 2018 TRLR45H and TRLR70USH trailers because the center-mounted jack may collapse under excessive load, increasing the risk of injury.
FHC, Inc. is recalling the microTargeting Drive System because the Depth Stop Adapter may damage implanted leads if over-tightened, potentially requiring replacement.
FHC, Inc. is recalling the microTargeting Drive System because the Depth Stop Adapter can damage implanted leads and stylets when over-tightened, requiring device replacement.
FHC, Inc. is recalling the microTargeting STar Drive System (Manual) because the Depth Stop Adapter may damage the lead and stylet if the screw is over-tightened.
FHC, Inc. is recalling the microTargeting Drive System because the Depth Stop Adapter can damage leads and stylets, potentially causing short circuits.
FHC, Inc. is recalling the Depth Stop Adapter because over-tightening the screw can damage implanted leads, causing short circuits and requiring replacement.
FHC, Inc. is recalling the Depth Stop Adapter because over-tightening the screw can damage implanted leads and stylets, requiring replacement.
FHC, Inc. is recalling Depth Stop Adapters because over-tightening the screw can damage implanted leads, requiring removal and replacement.
FHC, Inc. is recalling the microTargeting Drive System Depth Stop Adapter because over-tightening the screw can damage implanted leads, requiring replacement.
Ingenus Pharmaceuticals is recalling Irinotecan Hydrochloride Injection because of high out-of-specification assay values for potency.
Fagron Compounding Services is recalling 390 prefilled syringes of Neostigmine Methylsulfate Injection Solution because some may be incorrectly labeled with the wrong strength.
Fagron Sterile Services is recalling 840 prefilled syringes of Neostigmine Methylsulfate Injection Solution because they may be incorrectly labeled with the wrong strength.
FHC, Inc. is recalling 2,952 microTargeting Drive Systems because over-tightening the depth stop screw can damage implanted leads, requiring replacement.
Howmedica Osteonics Corp. is recalling specific LFIT Anatomic CoCr Femoral Heads because of a higher than expected number of complaints regarding disassociation from the hip stem.
FHC, Inc. is recalling the Depth Stop Adapter because over-tightening the screw can damage implanted leads, requiring surgical replacement.
FHC, Inc. is recalling the microTargeting Drive System Depth Stop Adapter because over-tightening the screw can damage implanted leads, requiring replacement.
FHC, Inc. is recalling microTargeting Lead Adapters because over-tightening the depth stop screw can damage implanted leads, requiring replacement.
Pierce is recalling 2007-2017 emergency vehicles because an aerial device bracket may detach and fall, potentially striking a person below.
Ingenus Pharmaceuticals is recalling specific lots of Irinotecan Hydrochloride Injection because they had high out-of-specification assay values for potency.