State
73,817 recalls have nationwide distribution and so reach Alabama. 6,378 additional recalls listed Alabama specifically in their distribution scope.
Of the 6,378 recalls naming Alabama we have scored against our rubric, 1,129 (18%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 1,605 (25%) are Severe.
Which agencies issued them
These figures cover only the 6,378 recalls whose distribution notice names Alabama specifically. The 73,817 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
Ford is recalling 2016-2017 Edge, MKX, and Continental vehicles because the driver's air bag may not fully inflate or detach during a crash.
Halcore Group is recalling 2017 Horton ambulances because overtightened rear brake bolts may cause loss of braking power, increasing crash risk.
Halcore Group is recalling 2017 AEV Traumahawk ambulances because overtightened rear brake bolts may cause loss of braking power, increasing crash risk.
Daimler Trucks North America is recalling 2017-2018 Thomas Built Buses Saf-T-Liner HDX school buses because a loose steering bolt may cause loss of vehicle control.
Tiffin is recalling 35 model-year 2012 Phaeton motorhomes because the exhaust pipe is mounted too close to the floor, creating a fire hazard.
Forest River is recalling 2017 Sandstorm and Stealth recreational vehicles because the liquid propane line may be damaged by the axle, creating a fire or explosion hazard.
Forest River is recalling 2017 Wildwood and Salem recreational trailers because an improperly installed refrigerator vent allows propane gas to enter the vehicle, increasing the risk of fire or explosion.
Gillig is recalling 1997-2017 Low Floor transit buses because front turn signals may not be sufficiently visible, increasing crash risk.
Little Tikes is recalling about 540,000 2-in-1 Snug 'n Secure Pink toddler swings because the plastic seat can crack or break, posing a fall hazard.
Carrier is expanding a recall for about 94,000 packaged terminal air conditioners and heat pumps because the power cord plug can overheat, posing a fire hazard.
Tiffin is recalling 2017 Allegro Open Road motorhomes because the tow hitch sticker lists incorrect weight capacities, which could lead to hitch failure.
General Motors is recalling 2017 Buick LaCrosse vehicles because water may enter the electric power steering connectors, potentially causing a loss of power steering.
BMW is recalling 2017 430i, 440i, M4, and Rolls-Royce Dawn vehicles because seat-mounted air bag inflator initiators may fail to ignite during a crash.
STIHL is recalling about 100,000 gas-powered chain saws because a leaking fuel line can cause fire and burn hazards. Consumers should stop using the saws and return them for a free repair.
Mercedes-Benz is recalling 307,629 vehicles because repeated starter attempts may overheat a component, increasing the risk of a fire.
Ready Pac Foods is recalling approximately 59,225 pounds of Puro Picante Blazin Hot chicken salad due to possible Listeria monocytogenes contamination. No illnesses have been reported.
GE Healthcare is recalling 60 Discovery MR450 MRI scanners because a component failure can cause the patient bore to heat up, potentially leading to serious burns.
Integra LifeSciences Corp. is recalling 944 units of the Cadence Total Ankle System because posterior tibial fractures have been reported.
Physio-Control is recalling 338 LIFEPAK 15 defibrillators because an internal relay may fail, preventing the device from delivering defibrillation energy.
Mako Surgical Corporation is recalling 595 Stryker Restoris RIO Reamer Handles because they may fail to engage mating components during surgery.
Zimmer Biomet is recalling 4,388 Comprehensive Reverse Shoulder System Humeral Trays because they are fracturing at higher-than-anticipated rates, posing a risk of revision surgery.
Argon Medical Devices is recalling specific bone marrow aspiration needles because a potential defect in the blister packaging may compromise the sterility of the product.
Aesculap Implant Systems LLC is recalling 24 GN200 Caiman HF generators due to a faulty component that may impact proper device functioning.
Atrium Medical Corporation is recalling Maquet Ocean Water Seal Chest Drains because the manual vent valve may fail to re-seal after use.
Atrium Medical Corporation is recalling Maquet Express Dry Seal Suction OCEAN DRAIN chest drains because the manual vent valve may fail to re-seal after use.