State
73,809 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 73,809 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
Ortovox is recalling about 20,000 avalanche transceivers because a software error may prevent them from transmitting survivor location data, delaying rescue efforts.
Badass Helmet Company is recalling Trooper motorcycle helmets that may not adequately protect the wearer in a crash or stay secured to the head.
Subaru is recalling 2018 Forester vehicles because the certification label may display incorrect wheel, tire, and air pressure data, potentially leading to improper tire installation.
Nissan is recalling 2007-2008 Versa sedans and hatchbacks because the passenger air bag inflators may explode. This defect could cause metal fragments to strike occupants, resulting in serious injury or death.
BMW is recalling 2018-2019 X3 and 2019 X4 vehicles because insufficient coating on rear brake caliper pistons may reduce braking performance.
Camso is recalling 2018 DTS 129 and Yeti Snow MX conversion kits because brake bolts can loosen, posing a crash or impact hazard.
Sandoz and Novartis are recalling about 470,000 blister packages of prescription drugs because the packaging failed to meet child-resistant closure requirements, posing a poisoning risk to children.
Entegra is recalling 2019 Emblem and Vision motorhomes because windshield wiper arms may lift at highway speeds, reducing visibility and increasing crash risk.
Entegra is recalling 2018-2019 motorhomes because incorrect cargo capacity labels may lead to vehicle overloading and increased crash risk.
Jayco is recalling 2019 White Hawk recreational trailers because screws securing ladder steps may break, posing a fall risk.
Jayco is recalling 2018-2019 Alante, Precept, Seneca, Redhawk, and Melbourne motorhomes because the cargo capacity label overstates limits, increasing crash risk.
Jayco is recalling 2019 Alante and Precept motorhomes because windshield wiper arms may lift at highway speeds, reducing visibility and increasing crash risk.
Keystone RV Company is recalling 2018-2019 Dutchmen Aerolite recreational trailers because the Federal Certification Label lists the wrong rim size, which could lead to unsafe rim replacements.
Philips is recalling 477 OmniDiagnost Classic X-ray systems because a broken tilt actuator could cause the table to rotate uncontrollably, posing a risk of injury.
Utz Quality Foods is recalling specific expiration dates of Utz Organic Yellow Corn Tortillas due to potential contamination with undeclared milk.
Utz Quality Foods is recalling specific expiration dates of Utz Organic Blue Corn Tortillas due to potential contamination with undeclared milk.
Utz Quality Foods is voluntarily recalling select tortilla chip items due to potential contamination with undeclared milk allergen.
Konica Minolta is recalling CS-7 medical devices because the Panasonic Toughbook laptops used in some configurations have a potential battery ignition risk.
Konica Minolta is recalling ImagePilot D9MA units because the Panasonic Toughbook laptops used in some configurations may experience battery ignition.
Utz Quality Foods is voluntarily recalling select tortilla chip products due to potential contamination with undeclared milk allergen.
Utz Quality Foods is voluntarily recalling select Golden Flake tortilla chips due to potential contamination with undeclared milk allergen.
Utz Quality Foods is voluntarily recalling select tortilla chip items due to potential contamination with undeclared milk allergen.
Philips is recalling 508 OmniDiagnost-Eleva X-ray systems because a broken actuator fixation can cause the table to rotate uncontrollably, posing a risk of injury.
St Jude Medical is recalling Promote Quadra implantable cardiac devices to release new firmware that strengthens security against unauthorized access.
St Jude Medical is recalling Fortify ICDs and CRT-Ds to release new firmware that strengthens security against unauthorized access. Older devices may require permanent disabling of RF communication.