State
73,722 recalls have nationwide distribution and so reach Alabama. 6,377 additional recalls listed Alabama specifically in their distribution scope.
Of the 6,377 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 1,604 (25%) are Severe.
Which agencies issued them
These figures cover only the 6,377 recalls whose distribution notice names Alabama specifically. The 73,722 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
Aston Martin is recalling specific 2017-2020 models because front seat air bag fasteners may not be tightened correctly, increasing injury risk.
General Motors is recalling 2018 Cadillac, Chevrolet, and GMC vehicles because a vacuum pump issue can reduce power brake assist, increasing stopping distance.
Jayco is recalling 2021 Jay Feather X213 trailers because incorrect tire and weight labels may lead to vehicle overloading.
The Protein Shoppe is recalling Red-E Tablets found to contain sildenafil, an unapproved drug for erectile dysfunction. The product was marketed without FDA approval.
Ford is recalling 2020 F-350 trucks with ambulance prep packages because incorrect rear axles were installed, creating a risk of tire blowouts.
Siemens is recalling Syngo.via RT Image Suite software due to a calibration offset error that could result in incorrect radiation dose or dose applied to the wrong location.
STIHL is recalling about 185,000 mini-cultivator attachments because the gearbox may be installed upside down, causing tines to rotate toward the operator and posing a laceration risk.
BMW is recalling approximately 312 certain 2020-2021 BMW models due to rearview camera software that may slightly obscure the rear view image, potentially increasing crash risk if drivers rely solely on the camera.
LivaNova is recalling 94 Perceval Single Use Accessory Kits because the Dual Collapser component may fail to reduce the heart valve diameter, preventing implantation.
ArthroCare Corporation is voluntarily recalling 15,559 units of Smith&Nephew SmartStitch PerfectPasser Connectors because a manufacturing error may cause the upper jaw to detach during use.
LivaNova is recalling 77 Perceval Single Use Accessory Kits because the Dual Collapser component may fail to reduce the heart valve diameter during implantation.
BMW is recalling certain 2020-2021 models due to debris in hybrid battery cells that could cause fire or injury. Owners are instructed not to charge vehicles or drive in manual mode.
Irvine Biomedical is recalling 40 units of Inquiry Steerable Diagnostic Catheters because packages were mislabeled with the wrong model and lot numbers, potentially causing procedure delays.
LivaNova is recalling 102 Perceval Single Use Accessory Kits because the Dual Collapser component may fail to reduce the heart valve diameter, preventing implantation.
Tesla is recalling 2020 Model Y vehicles with specific configurations because a software error prevents trailer brake lights from illuminating, increasing crash risk.
Perrigo is recalling 7.8 million Albuterol Sulfate inhalers nationwide because the delivery system may fail to dispense the medication.
Petzl is recalling approximately 14,850 low-stretch kernmantle ropes sold in the U.S. and Canada because deep cuts or tape securing rope ends can cause failure, posing fall and injury hazards.
Hologic is recalling 607 Panther Fusion Tube Trays because they may leak, potentially invalidating patient results or causing false negatives in flu and RSV assays.
Jayco is recalling 2021 Entegra motorhomes with Villa power seats because the electrical wiring may become damaged or chafed, causing short circuits and fire risk.
Suzuki is recalling 2018 GSX250R and GSX250RZ motorcycles because the headlight may fail, reducing visibility and increasing crash risk.
LivaNova is recalling specific lots of the Perceval Dual Collapser because complaints indicate the device may fail to collapse the heart valve during implantation.
LivaNova is recalling specific lots of Perceval Single Use Accessory Kits because the Dual Collapser component may fail to reduce the heart valve diameter during implantation.
ArthroCare is recalling Speed Stitch Needle Cassettes because a supplier error may have resulted in needles made of titanium instead of stainless steel, posing a risk of breakage during use.
Bio-Rad is recalling BioPlex 2200 Syphilis Total & RPR kits because of increased RPR reactivity levels in the kit material.
Irvine Biomedical is recalling 15 units of Inquiry Steerable Diagnostic Catheters because packages were mislabeled with the wrong model and batch numbers.