State
73,737 recalls have nationwide distribution and so reach Louisiana. 6,965 additional recalls listed Louisiana specifically in their distribution scope.
Of the 6,965 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 1,739 (25%) are Severe.
Which agencies issued them
These figures cover only the 6,965 recalls whose distribution notice names Louisiana specifically. The 73,737 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
Ford is recalling 2019-2020 Mustang and 2019 Expedition vehicles because the 'Transmission Not In Park' warning is shorter than intended, which may increase the risk of unintended vehicle movement.
McNeilus is recalling certain CNG fuel systems sold as aftermarket parts because the pressure relief devices may fail to vent during heat exposure, potentially causing the system to rupture.
Navistar is recalling 2018-2020 International LT and 2019-2020 RH trucks because a wrist pin bushing failure may cause unexpected engine shutdown and increase crash risk.
General Motors is recalling 2,281 vehicles due to potential loss of electric power steering assist caused by connector corrosion.
Sobeauty is recalling Mag Cube magnetic ball sets because the small, high-powered magnets pose a serious risk of intestinal injury or death if swallowed by children.
Noah Clothing is recalling men's reverse fleece hoodies because they fail federal flammability standards, posing a burn risk. No injuries have been reported.
Autocar is recalling 2016-2020 Xpeditor vehicles because the traction control system may malfunction without warning, increasing crash risk.
Fully Popped is recalling Poppin' Cobs 10 Pack Microwave Popcorn because the paper bags can catch fire in the microwave, posing fire and burn hazards.
Whole Foods Market is recalling Minestrone Soup sold in deli containers and bags because it may contain undeclared milk.
Philips North America is recalling 346 TraumaDiagnost X-Ray systems because a shaft may break due to material fatigue, causing the arm to fall and potentially injure patients or staff.
Vascular Solutions is recalling Langston Dual Lumen Catheters because the inner lumen may separate from the hub during pressure injection.
Amneal Pharmaceuticals is recalling Nizatidine Oral Solution because it may contain N-Nitrosodimethylamine (NDMA) levels above FDA limits.
B. Braun Medical Inc. is recalling one lot of Ceftazidime for Injection USP and Dextrose for Injection USP because the product failed stability specifications for high molecular weight polymers.
Elekta Inc is recalling 96 MONACO RTP systems because the software may alter contour shapes, potentially resulting in inaccurate radiation dose delivery to patients.
Prepac is recalling approximately 21,000 4-drawer chests because they can tip over if not anchored, posing serious hazards to children.
Welch Allyn is recalling X12+ Telemeters and patient cables because they may not meet defibrillation withstand requirements.
Allied Vision Group is recalling specific lots of Alcon Air Optix Night & Day Aqua contact lenses because potentially counterfeit products and packaging were imported to the U.S.
Stryker Sustainability Solutions is recalling 90 reprocessed Zimmer tourniquet cuffs because they are potentially mislabeled. The mislabeling could lead to device misuse or inadequate limb compression during surgery.
Philips is recalling 162 Azurion 7 M20 angiographic X-ray systems because unspecified torque on C-arm roll motor screws could cause them to become loose.
GE Healthcare is recalling 123 Lunar iDXA Advance bone densitometers because a control panel issue may cause the start button to stick, potentially leading to accidental radiation exposure.
Ocean Spray is recalling 5.5 oz cans of Pink Lite Cranberry Juice Drink because they contain undeclared sulfites. Consumers should stop using the product.
Welch Allyn is recalling ELI PC Service software because it may not meet defibrillation withstand safety requirements for medical electrical equipment.
Uromedica Inc. is recalling 11 ProACT Implantation Instrument Sets because defective U-channel sheaths may damage ProACT implant devices during use.
GE Healthcare is recalling 123 Lunar iDXA bone densitometers because a control panel defect may cause the start button to stick, potentially leading to accidental radiation exposure.
Kerr/Pentron is recalling 111 trial kits of Nexus Universal with OptiBond Universal due to a packaging error that included the incorrect bonding agent, potentially increasing the risk of bond failures.