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.
Nutrizone LLC is recalling all packages of Cali Green Malay Kratom because dietary supplements may be contaminated with Salmonella.
Nutrizone LLC is recalling all packages of Pain Out Maeng Da Kratom dietary supplements nationwide due to the potential for Salmonella contamination.
Nutrizone LLC is recalling all packages of Cali Thai Kratom because dietary supplements may be contaminated with Salmonella.
Nutrizone LLC is recalling all packages of Nirvanio Special Reserve Kratom because dietary supplements can be contaminated with Salmonella.
Nutrizone LLC is recalling all packages of Cali Maeng Da Kratom dietary supplements nationwide due to the potential for Salmonella contamination.
Lakota is recalling 2018-2019 Bighorn, Charger, and Colt trailers because ramp-securing bolts may loosen or break, increasing the risk of injury or a crash.
Divinity Product Distribution LLC is recalling kratom capsules because the ingredient lacks adequate safety information to ensure it does not present a significant risk of illness or injury.
Divinity Product Distribution LLC is recalling kratom powder products because the ingredient lacks sufficient safety data to ensure it does not pose a risk of illness or injury.
Lakota is recalling 2018-2019 Bighorn, Charger, and Colt trailers because missing hardware may allow the rear ramp to detach while moving, increasing crash risk.
Volkswagen is recalling 2018 Tiguan long wheelbase vehicles because a rear shock absorber loop may separate, potentially causing loss of vehicle control.
Philips is recalling 119 Brilliance Big Bore CT systems because closing the Emergency Stop may disable the horizontal motor, allowing the couch to move during patient load or unload.
Philips is recalling Panorama 1.0T MRI scanners due to a potential risk of helium gas release into the examination room during a magnet quench.
Philips is recalling 8,205 Multiva MRI systems worldwide due to a potential risk of helium gas release in the examination room during a magnet quench.
Draeger Medical Systems is recalling Infinity Acute Care System monitoring solutions because invasive pressure alarms may not activate.
Getinge is recalling 170 automated loading/unloading accessories for Washer-Disinfector 86 Series units due to a risk of disinfected goods falling to the floor.
Carefusion 2200 Inc is recalling 1,200 sterile thoracentesis and paracentesis kits because their packaging integrity may be compromised.
Funky Chunky LLC is recalling Chocolate Pretzels because they may contain undeclared tree nuts and peanuts. The recall covers 172 lbs of product distributed nationwide.
Philips is recalling Ingenia 1.5T CX MRI scanners due to a potential risk of helium gas release into the examination room during a magnet quench.
Philips is recalling the SmarthPath to dStream conversion software for 1.5T MRI systems due to a potential risk of helium gas release during a magnet quench.
Philips is recalling Brilliance 6 Slice CT systems because closing the Emergency Stop may disable the horizontal motor, allowing the couch to move during patient loading.
Philips is recalling 8,205 Multiva MRI systems worldwide due to a potential risk of helium gas release during a magnet quench.
Philips is recalling 8,205 Intera 1.0T MRI systems worldwide due to a potential risk of helium gas release during a magnet quench.
Philips is recalling 172 Ingenuity CT systems because closing the Emergency Stop may disable the horizontal motor, allowing the couch to move during patient load or unload.
Philips is recalling two Brilliance 16 Slice CT systems because the emergency stop may fail to disable the horizontal motor, allowing the couch to move during patient loading.
Carefusion 2200 Inc is recalling 14,200 Jamshidi (TJ) needles because the integrity of the sterile packaging is potentially compromised.