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.
Grand Design RV is recalling 95 model year 2022-2023 Solitude and 2023 Momentum fifth wheel trailers because loose or missing fasteners can let the refrigerator move and crack the propane line.
About 83,500 Belkin power banks and wireless charging stands are being recalled because the lithium-ion battery can overheat; one US fire and 15 international reports have been received.
About 32,600 Great Lakes Select button cell and coin battery packs are being recalled because they lack the child-resistant packaging and warning labels required under Reese's Law.
About 68,000 Trek and Electra bicycles with coaster brakes, plus replacement rear wheels, are being recalled because the coaster brakes can fail to engage.
International Motors is recalling 142 model year 2023-2027 IC Bus CESB school buses because the bus may exceed its Gross Vehicle Weight Rating when fully occupied with full tanks.
Honda is recalling 256,603 model year 2023-2025 Accord Hybrid vehicles because a software error may reset the integrated control module CPU while driving, causing a loss of drive power.
Forest River Bus is recalling certain 2025-2027 school buses because wheelchair restraints may fail to lock, increasing injury risk.
Forest River Bus is recalling 2025-2026 transit buses because wheelchair restraints may fail to lock, increasing injury risk.
About 700 Zigjoy toddler sleep sacks with feet are being recalled because they violate the mandatory flammability standard for children's sleepwear.
About 380 Bettina Doll Sets with Magic Light Unicorn are being recalled because the unicorn's battery compartment lets children easily access button cell batteries.
Integra LifeSciences is recalling 5,109 CODMAN Disposable Perforators, 9mm, extending an existing 14 mm recall for inadequate welds. The FDA has classified it Class I.
Tandem Diabetes Care is recalling 17,745 Tandem Mobi insulin pumps because a software issue can trigger a false vibration motor failure that halts insulin delivery. The FDA classified it Class I.
Integra LifeSciences is recalling 16,251 CODMAN Disposable Perforators, 11mm, extending an existing 14 mm recall for inadequate welds. The FDA has classified it Class I.
Yamaha is recalling 2,715 XMAX scooters because a camshaft bolt may loosen, causing engine stalls and increasing crash risk.
Volkswagen Group of America is recalling certain 2025 Audi Q7, Q8, SQ8 and RS Q8 vehicles because the front seat belt buckles may be missing a rivet that secures the buckle to the stalk.
AquaStar is recalling 3,600 cases of Kroger Mercado Cooked Medium Peeled Tail-Off Shrimp because the shrimp may be contaminated with Cesium-137.
AquaStar is recalling 1,800 cases of AquaStar 13/15 Raw Shrimp Easy Peel Deveined, sold at Publix, because the shrimp may be contaminated with Cesium-137.
AquaStar is recalling 3,600 cases of Waterfront Bistro Frozen Raw EZ-Peel White Shrimp 21/25 because the shrimp may be contaminated with Cesium-137.
AquaStar is recalling 1,458 cases of Publix Extra Large Shrimp Easy to Peel Deveined 21/25 because the shrimp may be contaminated with Cesium-137.
Zydus Pharmaceuticals is recalling clomiPRAMINE Hydrochloride Capsules USP 50 mg after N-Nitroso Desmethyl-Clomipramine was found above the FDA acceptable intake limit.
AquaStar is recalling 5,400 cases of Kroger Raw Colossal EZ Peel Shrimp because the shrimp may be contaminated with Cesium-137.
Zydus Pharmaceuticals is recalling clomiPRAMINE Hydrochloride Capsules USP 75 mg after N-Nitroso Desmethyl-Clomipramine was found above the FDA acceptable intake limit.
Zydus Pharmaceuticals is recalling clomiPRAMINE Hydrochloride Capsules USP 25 mg after N-Nitroso Desmethyl-Clomipramine was found above the FDA acceptable intake limit.
Mozarc Medical is recalling 3,258 MAHURKAR acute high pressure triple lumen catheter trays with straight extensions, 12 Fr x 24 cm, over header bag seal integrity.
Beckman Coulter is recalling 2,932 units of SYNCHRON Systems Direct LDL Cholesterol reagent from one lot because it may generate false high results.