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.
Polaris is recalling about 10,900 Ranger XP recreational off-highway vehicles because the center seat belt bracket can separate from the frame, posing an injury hazard to riders.
Kumho is recalling specific Solus KH16 tires because the belts may separate under severe conditions, increasing the risk of a crash.
Daimler Trucks North America is recalling 2014-2018 Thomas Built Buses school buses because a wall mounting bracket may crack, increasing injury risk in a crash.
Base Brands is recalling Reduce Hydro Pro water bottles because the pink paint on the bear design exceeds federal lead paint standards.
BMW is recalling 2007-2012 models because a failing electric auxiliary water pump can overheat the circuit board, increasing the risk of a fire.
Fresenius Medical Care is recalling Liberty Select Cyclers due to a software issue that may cause overfill, posing a risk of serious injury or death.
Volkswagen is recalling 2006-2007 Passat sedans and wagons because the driver's air bag inflator may explode during deployment, posing a risk of serious injury or death.
W & H DentalWerk is recalling S-N1 and S-N2 foot controls because they may fail to stop the motor, posing a risk of serious patient injury.
Terumo is recalling 2,677 Cardiovascular Procedure Kits containing Pall LG6NS filters due to a risk of blood leaks through the hydrophobic portion.
Reliance Medical Products is recalling 933 Refractor Suspension Arms because missing parts caused the device to fall on a patient.
Poppies International is recalling three brands of frozen Belgian mini eclairs because they may be contaminated with Listeria monocytogenes.
ICU Medical is recalling 250 pouches of 7-inch intravascular administration sets because they were manufactured with an incorrect spin collar.
Teleflex Medical Europe Ltd is recalling 107,962 latex rebreathing bags because they lack the required warning that the product contains natural rubber latex, which may cause allergic reactions.
C.R. Bard is recalling specific lots of Bard Adult/Pediatric Feeding Tubes because the tubing and ENFit connector may not be fused effectively.
Newmar is recalling specific 2013-2017 motorhomes because low beam headlights turn off when high beams are activated, reducing driver visibility.
Getinge is recalling 5,214 VOLISTA StandOP surgical lights because the central handle holder can detach, potentially dropping particles into the sterile field during procedures.
C.R. Bard is recalling 23,400 infant feeding tubes because the tubing and connector may not be effectively fused.
Beckman Coulter is recalling 288 AQUIOS CL Flow Cytometer Systems because the single tube loader may process the same sample with two different IDs, potentially causing erroneous results.
Primark is recalling about 14,500 decorative cushions sold in the northeastern U.S. because they can catch fire if exposed to an ignition source.
Hill-Rom is recalling 2,117 Progressa adjustable hospital beds because a braking system component may break, causing unwanted bed movement and potential injury.
Riverside RV is recalling 2015-2017 White Water, Water Fall, and Mt. McKinley motorhomes because certain fire extinguishers may clog or detach, posing injury risks.
C.R. Bard is recalling specific lots of Bard Premature Infant Feeding Tubes because the tubing and ENFit connector may not be effectively fused.
Beckman Coulter is recalling iQ200 Series Urine Microscopy Analyzers because they may fail to read dilution barcodes, causing erroneous results that could delay treatment.
C.R. Bard is recalling 42,200 units of Bard Premature Infant Feeding Tubes due to potentially ineffective fusion between the tubing and the ENFit connector.
Elroselabs Inc. is voluntarily recalling Molleave, 2 oz bottles, due to current Good Manufacturing Practice (cGMP) deviations. The product was distributed nationwide.