State
73,809 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 73,809 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
Pharmedium Services, LLC is voluntarily recalling 60 bags of compounded Oxytocin injection because the drug was found to be subpotent.
Banner Pharmacy Services is recalling fentanyl citrate infusion cassettes due to a lack of assurance of sterility. The affected products were distributed nationwide.
Pharmedium Services is voluntarily recalling 42 bags of compounded Oxytocin 40 units in Lactated Ringer's solution because the drug was subpotent.
General Mills is recalling specific lots of Cascadian Farm Organic Cinnamon Raisin Granola because they contain undeclared almonds, a major food allergen.
Pharmedium Services, LLC is voluntarily recalling 4,452 bags of compounded Oxytocin 30 units due to subpotent drug levels. The FDA classified this as a Class II recall.
Banner Pharmacy Services is recalling specific lots of Hydromorphone HCl syringes because the FDA determined there is a lack of assurance of sterility.
Banner Pharmacy Services is recalling 3,136 bags of Vancomycin 1.5 grams in 0.9% Sodium Chloride due to a lack of assurance of sterility.
Pharmedium Services, LLC is voluntarily recalling 763 bags of compounded Oxytocin 30 units in Lactated Ringer's USP. The recall was initiated because the drug was found to be subpotent.
Banner Pharmacy Services is recalling 481 bags of Norepinephrine Bitartrate in 0.9% Sodium Chloride due to a lack of assurance of sterility.
Banner Pharmacy Services is recalling Oxytocin 30 units in 0.9% Sodium Chloride bags because the FDA determined there is a lack of assurance of sterility.
Heartland is recalling 2018 Prowler and Trail Runner trailers because electric brake wires may be severed by spring hangers, increasing crash risk.
Banner Pharmacy Services is recalling fentanyl citrate syringes because the agency could not ensure the product was sterile.
Pharmedium Services, LLC is voluntarily recalling Oxytocin 20 units in Lactated Ringer's Injection USP bags because the drug was found to be subpotent.
Pharmedium Services, LLC is voluntarily recalling 2,232 bags of compounded Oxytocin injection because the drug was found to be subpotent.
Pharmedium Services, LLC is voluntarily recalling 1,152 bags of compounded Oxytocin 40 units in Lactated Ringer's USP because the drug was subpotent.
Nissan is recalling 2017-2018 Infiniti QX30 vehicles because the driver's air bag may deploy unexpectedly due to steering component grounding issues.
Pharmedium Services, LLC is voluntarily recalling 390 bags of compounded Oxytocin 20 units in Lactated Ringer's Injection due to subpotent drug levels.
Little Mass is recalling about 2,300 children's nightgowns and pajama sets because they fail to meet federal flammability standards, posing a risk of burn injuries.
Heartland is recalling 2018 Pioneer recreational trailers because the propane manifold block may be mounted too close to the shackle, creating a leak risk.
Nucletron BV is recalling Oncentra Brachy 4.5 radiation therapy software because incorrect source step sizes may occur in treatment plans.
VIV&LUL is recalling about 950 children's pajama sets sold on Amazon.com because they fail to meet federal flammability standards, posing a risk of burn injuries.
Pharmedium Services, LLC is voluntarily recalling 978 bags of compounded Oxytocin in Lactated Ringer's Injection because the drug was subpotent.
Dondolo is recalling about 3,100 children's nightgowns and pajama sets because they fail to meet federal flammability standards, posing a burn risk.
Sysmex America is recalling Fluorocell PLT reagent lots because they may produce falsely low platelet results, potentially affecting diagnostic accuracy.
Encore Medical is recalling 46 EMPOWR PS Knee Inserts because one unit was packaged with the wrong implant. The recall covers US nationwide distribution.