State
72,940 recalls have nationwide distribution and so reach Louisiana. 6,922 additional recalls listed Louisiana specifically in their distribution scope.
Of the 6,922 recalls naming Louisiana we have scored against our rubric, 1,094 (16%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 1,483 (21%) are Severe.
Which agencies issued them
These figures cover only the 6,922 recalls whose distribution notice names Louisiana specifically. The 72,940 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
Frontier Devices 14 mm Distraction Pins in 10 single packs are recalled because the labeling includes a shelf life that has not been validated. 10,960 units are affected.
Frontier Devices 12 mm Distraction Pins in 10 double packs are recalled because the labeling includes a shelf life that has not been validated. 160 units are affected.
Hi-Tech Pharmaceuticals Joint-RX dietary supplement, 90 count, lot 503110607, is recalled for unapproved drug claims. The recall covers 85,950 units across the firm's affected products.
Frontier Devices 14 mm Distraction Pins in 5 single packs are recalled because the labeling includes a shelf life that has not been validated. 2,700 units are affected.
Sulfamethoxazole and Trimethoprim Tablets, USP 800 mg/160 mg double strength, in 6, 10, 14 and 20-count bottles are recalled because a micro-organism was found on a lot of packaging coil.
PrimeNutrition Phytoform Fruits & Greens Formula in watermelon, 13.75 oz, lot 174271126, is recalled for unapproved drug claims and misbranding. The recall covers 85,950 units across the firm's affected products.
Hi-Tech Pharmaceuticals Pine Bark, 60 tablets, lot C15Cl4, is recalled for unapproved drug claims and misbranding. The recall covers 85,950 units across the firm's affected products.
Frontier Devices 16 mm Distraction Pins in 10 single packs are recalled because the labeling includes a shelf life that has not been validated. 490 units are affected.
Frontier Devices 12 mm Distraction Pins in 10 single packs are recalled because the labeling includes a shelf life that has not been validated. 3,790 units are affected.
Chlorpromazine Hydrochloride Tablets, USP, 200 mg, in blister cartons from American Health Packaging, are recalled because a micro-organism was found on a lot of packaging coil. 873 cartons are affected.
PrimeNutrition Taurine, 8.12 oz, lot 710581618, is recalled for unapproved drug claims and misbranding. The recall covers 85,950 units across the firm's affected products.
Hi-Tech Pharmaceuticals Fish Oil, 90 soft gels, lot 517120551, is recalled for unapproved drug claims. The recall covers 85,950 units across the firm's affected products.
Chlorpromazine Hydrochloride Tablets, USP, 50 mg, in blisterpacks from American Health Packaging, are recalled because a micro-organism was found on a lot of packaging coil. 1,062 cartons are affected.
Six vials of Sandoz Cyclophosphamide Injection 500 mg/5 mL from lot 110459 are recalled nationwide after a temperature excursion during transportation.
MEDITECH Expanse Laboratory modules are recalled because entering multiple keys that trigger input simultaneously may remove data from the first field of screens or questionnaires. 148 units are affected.
i-STAT CG8+ cartridges are recalled across all lots for lack of a 510(k) premarket clearance reflecting updated sample types and measurement ranges. 8,962,450 units are affected.
iForce Nutrition Joint Help dietary supplement, 120 capsules, lot 101330812, is recalled for unapproved drug claims. The recall covers 85,950 units across the firm's affected products.
i-STAT EG7+ cartridges are recalled across all lots for lack of a 510(k) premarket clearance reflecting updated sample types and measurement ranges. 6,115,950 units are affected.
Frontier Devices 14 mm Distraction Pins in 10 double packs are recalled because the labeling includes a shelf life that has not been validated.
Lamborghini is recalling 2025 Urus vehicles because improperly tightened fuel pump fasteners may cause a fuel leak, increasing the risk of fire.
Blue Bird is recalling 2021-2026 Vision school and transit buses because brake software may activate the parking brake unexpectedly, increasing crash risk.
BMW is recalling certain 2019-2022 BMW models and the Toyota Supra because the engine starter relay may corrode, overheat and short circuit. Owners are told to park outside until repaired.
Porsche is recalling certain 2024–2026 Cayenne and Panamera models because fasteners securing the high pressure fuel pump may not be tightened properly, creating a fuel leak risk and potential fire hazard.
Ford is recalling certain 2020-2021 F-250, F-350 and F-450 vehicles because the steering column upper shaft may detach from the steering column, causing a loss of steering control.
New Flyer is recalling 2019-2025 XE35, XE40, and XE60 transit buses because a high voltage battery short circuit may cause a fire. Owners should park outside and limit charging to 75%.